Canonical Allele Identifier: CA344552776

Gene: CD46 MIR29B2CHG

Linked Data

• MyVariant Identifiers: chr1:g.207958444T>G (hg19) ; chr1:g.207785099T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207785099T>G , CM000663.2:g.207785099T>G	GRCh38
NC_000001.10:g.207958444T>G , CM000663.1:g.207958444T>G	GRCh37
NC_000001.9:g.206025067T>G	NCBI36
NG_009296.1:g.38043T>G , LRG_155:g.38043T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490278.2:n.2185T>G (CD46)
ENST00000496723.2:n.1762T>G (CD46)
ENST00000636114.2:n.2704T>G (CD46)
ENST00000695777.1:c.1011T>G (CD46)	ENSP00000512167.1:p.Ile337Met
ENST00000695778.1:c.966T>G (CD46)	ENSP00000512168.1:p.Ile322Met
ENST00000695779.1:n.1728T>G (CD46)
ENST00000695780.1:c.938-557T>G (CD46)	ENSP00000512169.1:n.938-557T>G
ENST00000695781.1:c.*94T>G (CD46)	ENSP00000512170.1:n.*94T>G
ENST00000695782.1:c.966T>G (CD46)	ENSP00000512171.1:p.Ile322Met
ENST00000695783.1:n.4379T>G (CD46)
ENST00000695784.1:c.*137T>G (CD46)	ENSP00000512172.1:n.*137T>G
ENST00000695786.1:n.933T>G (CD46)
ENST00000695787.1:n.2369T>G (CD46)
ENST00000695788.1:n.590T>G (CD46)
ENST00000695789.1:n.2262T>G (CD46)
ENST00000695790.1:n.2251T>G (CD46)
ENST00000367042.6:c.1011T>G (CD46) MANE Select	ENSP00000356009.1:p.Ile337Met
ENST00000636114.1:n.765T>G (CD46)
ENST00000322875.8:c.1056T>G (CD46)	ENSP00000313875.4:p.Ile352Met
ENST00000322918.9:c.966T>G (CD46)	ENSP00000314664.5:p.Ile322Met
ENST00000354848.5:c.1011T>G (CD46)	ENSP00000346912.1:p.Ile337Met
ENST00000357714.5:c.966T>G (CD46)	ENSP00000350346.1:p.Ile322Met
ENST00000358170.6:c.1056T>G (CD46)	ENSP00000350893.2:p.Ile352Met
ENST00000360212.6:c.924T>G (CD46)	ENSP00000353342.2:p.Ile308Met
ENST00000367041.5:c.966T>G (CD46)	ENSP00000356008.1:p.Ile322Met
ENST00000367042.5:c.1011T>G (CD46)	ENSP00000356009.1:p.Ile337Met
ENST00000367047.5:c.867T>G (CD46)	ENSP00000356014.1:p.Ile289Met
ENST00000462968.2:c.92T>G (CD46)
ENST00000469535.5:n.5760T>G (CD46)
ENST00000471987.1:n.121T>G (CD46)
ENST00000480003.5:c.969T>G (CD46)	ENSP00000418471.1:p.Ile323Met
ENST00000488596.5:n.390T>G (CD46)
NM_002389.4:c.1056T>G , LRG_155t1:c.1056T>G (CD46)	NP_002380.3:p.Ile352Met
NM_153826.3:c.1011T>G (CD46)	NP_722548.1:p.Ile337Met
NM_172350.2:c.966T>G (CD46)	NP_758860.1:p.Ile322Met
NM_172351.2:c.1011T>G (CD46)	NP_758861.1:p.Ile337Met
NM_172352.2:c.966T>G (CD46)	NP_758862.1:p.Ile322Met
NM_172353.2:c.966T>G (CD46)	NP_758863.1:p.Ile322Met
NM_172359.2:c.1056T>G (CD46)	NP_758869.1:p.Ile352Met
NM_172361.2:c.924T>G (CD46)	NP_758871.1:p.Ile308Met
XM_011509563.1:c.1014T>G (CD46)	XP_011507865.1:p.Ile338Met
XM_011509564.1:c.969T>G (CD46)	XP_011507866.1:p.Ile323Met
XR_922496.1:n.7666+20906A>C (MIR29B2CHG)
XR_922497.1:n.6306-22111A>C (MIR29B2CHG)
NM_172355.2:c.969T>G (CD46)	NP_758865.1:p.Ile323Met
NM_172356.2:c.969T>G (CD46)	NP_758866.1:p.Ile323Met
NM_172357.2:c.924T>G (CD46)	NP_758867.1:p.Ile308Met
NM_172358.2:c.1011T>G (CD46)	NP_758868.1:p.Ile337Met
XM_011509563.2:c.1014T>G (CD46)	XP_011507865.1:p.Ile338Met
XM_017001308.2:c.1014T>G (CD46)	XP_016856797.1:p.Ile338Met
XR_001737177.2:n.2162T>G (CD46)
XR_002956621.1:n.2700T>G (CD46)
XR_002956622.1:n.2700T>G (CD46)
NM_153826.4:c.1011T>G (CD46)	NP_722548.1:p.Ile337Met
NM_172350.3:c.966T>G (CD46)	NP_758860.1:p.Ile322Met
NM_172351.3:c.1011T>G (CD46) MANE Select	NP_758861.1:p.Ile337Met
NM_172352.3:c.966T>G (CD46)	NP_758862.1:p.Ile322Met
NM_172353.3:c.966T>G (CD46)	NP_758863.1:p.Ile322Met
NM_172355.3:c.969T>G (CD46)	NP_758865.1:p.Ile323Met
NM_172356.3:c.969T>G (CD46)	NP_758866.1:p.Ile323Met
NM_172357.3:c.924T>G (CD46)	NP_758867.1:p.Ile308Met
NM_172358.3:c.1011T>G (CD46)	NP_758868.1:p.Ile337Met
NM_172359.3:c.1056T>G (CD46)	NP_758869.1:p.Ile352Met
NM_172361.3:c.924T>G (CD46)	NP_758871.1:p.Ile308Met