Canonical Allele Identifier: CA1139773213

Gene: CD46 MIR29B2CHG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207794374T= , CM000663.2:g.207794374T=	GRCh38
NC_000001.10:g.207967719T= , CM000663.1:g.207967719T=	GRCh37
NC_000001.9:g.206034342T=	NCBI36
NG_009296.1:g.47318T= , LRG_155:g.47318T=

Transcript Alleles

HGVS	Amino-acid Change
NM_172351.3:c.*897T= (CD46) MANE Select	NP_758861.1:n.*897T=
ENST00000367042.6:c.*897T= (CD46) MANE Select	ENSP00000356009.1:n.*897T=
NM_002389.4:c.*897T= , LRG_155t1:c.*897T= (CD46)	NP_002380.3:n.*897T=
NM_153826.3:c.*783T= (CD46)	NP_722548.1:n.*783T=
NM_153826.4:c.*783T= (CD46)	NP_722548.1:n.*783T=
NM_172350.2:c.*779T= (CD46)	NP_758860.1:n.*779T=
NM_172350.3:c.*779T= (CD46)	NP_758860.1:n.*779T=
NM_172351.2:c.*897T= (CD46)	NP_758861.1:n.*897T=
NM_172352.2:c.*897T= (CD46)	NP_758862.1:n.*897T=
NM_172352.3:c.*897T= (CD46)	NP_758862.1:n.*897T=
NM_172353.2:c.*783T= (CD46)	NP_758863.1:n.*783T=
NM_172353.3:c.*783T= (CD46)	NP_758863.1:n.*783T=
NM_172355.2:c.*897T= (CD46)	NP_758865.1:n.*897T=
NM_172355.3:c.*897T= (CD46)	NP_758865.1:n.*897T=
NM_172356.2:c.*783T= (CD46)	NP_758866.1:n.*783T=
NM_172356.3:c.*783T= (CD46)	NP_758866.1:n.*783T=
NM_172357.2:c.*897T= (CD46)	NP_758867.1:n.*897T=
NM_172357.3:c.*897T= (CD46)	NP_758867.1:n.*897T=
NM_172358.2:c.*779T= (CD46)	NP_758868.1:n.*779T=
NM_172358.3:c.*779T= (CD46)	NP_758868.1:n.*779T=
NM_172359.2:c.*783T= (CD46)	NP_758869.1:n.*783T=
NM_172359.3:c.*783T= (CD46)	NP_758869.1:n.*783T=
NM_172361.2:c.*783T= (CD46)	NP_758871.1:n.*783T=
NM_172361.3:c.*783T= (CD46)	NP_758871.1:n.*783T=
ENST00000322875.8:c.*783T= (CD46)	ENSP00000313875.4:n.*783T=
ENST00000322918.9:c.*779T= (CD46)	ENSP00000314664.5:n.*779T=
ENST00000354848.5:c.*783T= (CD46)	ENSP00000346912.1:n.*783T=
ENST00000357714.5:c.*783T= (CD46)	ENSP00000350346.1:n.*783T=
ENST00000358170.6:c.*897T= (CD46)	ENSP00000350893.2:n.*897T=
ENST00000360212.6:c.*783T= (CD46)	ENSP00000353342.2:n.*783T=
ENST00000367041.5:c.*897T= (CD46)	ENSP00000356008.1:n.*897T=
ENST00000367042.5:c.*897T= (CD46)	ENSP00000356009.1:n.*897T=
ENST00000367047.5:c.*783T= (CD46)	ENSP00000356014.1:n.*783T=
ENST00000462968.2:c.254-631T= (CD46)
ENST00000469535.5:n.6687T= (CD46)
ENST00000490278.2:n.3168T= (CD46)
ENST00000496723.2:n.2782T= (CD46)
ENST00000636114.1:n.1692T= (CD46)
ENST00000636114.2:n.3631T= (CD46)
ENST00000695777.1:c.*779T= (CD46)	ENSP00000512167.1:n.*779T=
ENST00000695778.1:c.*938T= (CD46)	ENSP00000512168.1:n.*938T=
ENST00000695779.1:n.2748T= (CD46)
ENST00000695780.1:c.*779T= (CD46)	ENSP00000512169.1:n.*779T=
ENST00000695781.1:c.*1021T= (CD46)	ENSP00000512170.1:n.*1021T=
ENST00000695782.1:c.*779T= (CD46)	ENSP00000512171.1:n.*779T=
ENST00000695783.1:n.5399T= (CD46)
ENST00000695784.1:c.*1064T= (CD46)	ENSP00000512172.1:n.*1064T=
ENST00000695786.1:n.1860T= (CD46)
ENST00000695788.1:n.1517T= (CD46)
ENST00000695790.1:n.3690T= (CD46)
XM_011509563.1:c.*783T= (CD46)	XP_011507865.1:n.*783T=
XM_011509563.2:c.*783T= (CD46)	XP_011507865.1:n.*783T=
XM_011509564.1:c.*783T= (CD46)	XP_011507866.1:n.*783T=
XM_017001308.2:c.*897T= (CD46)	XP_016856797.1:n.*897T=
XR_001737177.2:n.3089T= (CD46)
XR_002956621.1:n.3627T= (CD46)
XR_002956622.1:n.3720T= (CD46)
XR_922496.1:n.7666+11631A= (MIR29B2CHG)
XR_922497.1:n.6305+21555A= (MIR29B2CHG)