Canonical Allele Identifier: CA2559464710

Gene: CD46 MIR29B2CHG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207784855_207784856insCACT , CM000663.2:g.207784855_207784856insCACT	GRCh38
NC_000001.10:g.207958200_207958201insCACT , CM000663.1:g.207958200_207958201insCACT	GRCh37
NC_000001.9:g.206024823_206024824insCACT	NCBI36
NG_009296.1:g.37799_37800insCACT , LRG_155:g.37799_37800insCACT

Transcript Alleles

HGVS	Amino-acid change
ENST00000490278.2:n.1941_1942insCACT (CD46)
ENST00000496723.2:n.1734-216_1734-215insCACT (CD46)
ENST00000636114.2:n.2676-216_2676-215insCACT (CD46)
ENST00000695777.1:c.983-216_983-215insCACT (CD46)	ENSP00000512167.1:n.983-216_983-215insCACT
ENST00000695778.1:c.938-216_938-215insCACT (CD46)	ENSP00000512168.1:n.938-216_938-215insCACT
ENST00000695779.1:n.1700-216_1700-215insCACT (CD46)
ENST00000695780.1:c.938-801_938-800insCACT (CD46)	ENSP00000512169.1:n.938-801_938-800insCACT
ENST00000695781.1:c.*66-216_*66-215insCACT (CD46)	ENSP00000512170.1:n.*66-216_*66-215insCACT
ENST00000695782.1:c.938-216_938-215insCACT (CD46)	ENSP00000512171.1:n.938-216_938-215insCACT
ENST00000695783.1:n.4351-216_4351-215insCACT (CD46)
ENST00000695784.1:c.*109-216_*109-215insCACT (CD46)	ENSP00000512172.1:n.*109-216_*109-215insCACT
ENST00000695786.1:n.905-216_905-215insCACT (CD46)
ENST00000695787.1:n.2125_2126insCACT (CD46)
ENST00000695788.1:n.562-216_562-215insCACT (CD46)
ENST00000695789.1:n.2018_2019insCACT (CD46)
ENST00000695790.1:n.2007_2008insCACT (CD46)
ENST00000367042.6:c.983-216_983-215insCACT (CD46) MANE Select	ENSP00000356009.1:n.983-216_983-215insCACT
ENST00000636114.1:n.737-216_737-215insCACT (CD46)
ENST00000322875.8:c.1028-216_1028-215insCACT (CD46)	ENSP00000313875.4:n.1028-216_1028-215insCACT
ENST00000322918.9:c.938-216_938-215insCACT (CD46)	ENSP00000314664.5:n.938-216_938-215insCACT
ENST00000354848.5:c.983-216_983-215insCACT (CD46)	ENSP00000346912.1:n.983-216_983-215insCACT
ENST00000357714.5:c.938-216_938-215insCACT (CD46)	ENSP00000350346.1:n.938-216_938-215insCACT
ENST00000358170.6:c.1028-216_1028-215insCACT (CD46)	ENSP00000350893.2:n.1028-216_1028-215insCACT
ENST00000360212.6:c.896-216_896-215insCACT (CD46)	ENSP00000353342.2:n.896-216_896-215insCACT
ENST00000367041.5:c.938-216_938-215insCACT (CD46)	ENSP00000356008.1:n.938-216_938-215insCACT
ENST00000367042.5:c.983-216_983-215insCACT (CD46)	ENSP00000356009.1:n.983-216_983-215insCACT
ENST00000367047.5:c.839-216_839-215insCACT (CD46)	ENSP00000356014.1:n.839-216_839-215insCACT
ENST00000462968.2:c.64-216_64-215insCACT (CD46)
ENST00000469535.5:n.5732-216_5732-215insCACT (CD46)
ENST00000471987.1:n.93-216_93-215insCACT (CD46)
ENST00000480003.5:c.941-216_941-215insCACT (CD46)	ENSP00000418471.1:n.941-216_941-215insCACT
ENST00000488596.5:n.362-216_362-215insCACT (CD46)
NM_002389.4:c.1028-216_1028-215insCACT , LRG_155t1:c.1028-216_1028-215insCACT (CD46)	NP_002380.3:n.1028-216_1028-215insCACT
NM_153826.3:c.983-216_983-215insCACT (CD46)	NP_722548.1:n.983-216_983-215insCACT
NM_172350.2:c.938-216_938-215insCACT (CD46)	NP_758860.1:n.938-216_938-215insCACT
NM_172351.2:c.983-216_983-215insCACT (CD46)	NP_758861.1:n.983-216_983-215insCACT
NM_172352.2:c.938-216_938-215insCACT (CD46)	NP_758862.1:n.938-216_938-215insCACT
NM_172353.2:c.938-216_938-215insCACT (CD46)	NP_758863.1:n.938-216_938-215insCACT
NM_172359.2:c.1028-216_1028-215insCACT (CD46)	NP_758869.1:n.1028-216_1028-215insCACT
NM_172361.2:c.896-216_896-215insCACT (CD46)	NP_758871.1:n.896-216_896-215insCACT
XM_011509563.1:c.986-216_986-215insCACT (CD46)	XP_011507865.1:n.986-216_986-215insCACT
XM_011509564.1:c.941-216_941-215insCACT (CD46)	XP_011507866.1:n.941-216_941-215insCACT
XR_922496.1:n.7666+21152_7666+21153insGAGT (MIR29B2CHG)
XR_922497.1:n.6306-21865_6306-21864insGAGT (MIR29B2CHG)
NM_172355.2:c.941-216_941-215insCACT (CD46)	NP_758865.1:n.941-216_941-215insCACT
NM_172356.2:c.941-216_941-215insCACT (CD46)	NP_758866.1:n.941-216_941-215insCACT
NM_172357.2:c.896-216_896-215insCACT (CD46)	NP_758867.1:n.896-216_896-215insCACT
NM_172358.2:c.983-216_983-215insCACT (CD46)	NP_758868.1:n.983-216_983-215insCACT
XM_011509563.2:c.986-216_986-215insCACT (CD46)	XP_011507865.1:n.986-216_986-215insCACT
XM_017001308.2:c.986-216_986-215insCACT (CD46)	XP_016856797.1:n.986-216_986-215insCACT
XR_001737177.2:n.2134-216_2134-215insCACT (CD46)
XR_002956621.1:n.2672-216_2672-215insCACT (CD46)
XR_002956622.1:n.2672-216_2672-215insCACT (CD46)
NM_153826.4:c.983-216_983-215insCACT (CD46)	NP_722548.1:n.983-216_983-215insCACT
NM_172350.3:c.938-216_938-215insCACT (CD46)	NP_758860.1:n.938-216_938-215insCACT
NM_172351.3:c.983-216_983-215insCACT (CD46) MANE Select	NP_758861.1:n.983-216_983-215insCACT
NM_172352.3:c.938-216_938-215insCACT (CD46)	NP_758862.1:n.938-216_938-215insCACT
NM_172353.3:c.938-216_938-215insCACT (CD46)	NP_758863.1:n.938-216_938-215insCACT
NM_172355.3:c.941-216_941-215insCACT (CD46)	NP_758865.1:n.941-216_941-215insCACT
NM_172356.3:c.941-216_941-215insCACT (CD46)	NP_758866.1:n.941-216_941-215insCACT
NM_172357.3:c.896-216_896-215insCACT (CD46)	NP_758867.1:n.896-216_896-215insCACT
NM_172358.3:c.983-216_983-215insCACT (CD46)	NP_758868.1:n.983-216_983-215insCACT
NM_172359.3:c.1028-216_1028-215insCACT (CD46)	NP_758869.1:n.1028-216_1028-215insCACT
NM_172361.3:c.896-216_896-215insCACT (CD46)	NP_758871.1:n.896-216_896-215insCACT