Canonical Allele Identifier: CA2450541940

Gene: COL4A6

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108157054A= , CM000685.2:g.108157054A=	GRCh38
NC_000023.10:g.107400284A= , CM000685.1:g.107400284A=	GRCh37
NC_000023.9:g.107286940A=	NCBI36
NG_012059.2:g.287421T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334504.12:c.5019T= MANE Select	ENSP00000334733.7:p.Ala1673=
ENST00000334504.11:c.5019T=	ENSP00000334733.7:p.Ala1673=
ENST00000372216.8:c.5022T=	ENSP00000361290.4:p.Ala1674=
ENST00000394872.6:c.5070T=	ENSP00000378340.3:p.Ala1690=
ENST00000538570.5:c.4848T=	ENSP00000445236.1:p.Ala1616=
ENST00000545689.2:c.4983T=	ENSP00000443707.2:p.Ala1661=
ENST00000621266.4:c.4947T=	ENSP00000482970.1:p.Ala1649=
NM_001287758.1:c.5070T=	NP_001274687.1:p.Ala1690=
NM_001287759.1:c.4947T=	NP_001274688.1:p.Ala1649=
NM_001287760.1:c.4848T=	NP_001274689.1:p.Ala1616=
NM_001847.3:c.5022T=	NP_001838.2:p.Ala1674=
NM_033641.3:c.5019T=	NP_378667.1:p.Ala1673=
XM_006724617.2:c.5073T=	XP_006724680.1:p.Ala1691=
XM_011530852.1:c.5001T=	XP_011529154.1:p.Ala1667=
XM_011530853.1:c.4989T=	XP_011529155.1:p.Ala1663=
XM_006724617.3:c.5073T=	XP_006724680.1:p.Ala1691=
XM_011530852.2:c.5001T=	XP_011529154.1:p.Ala1667=
XM_011530853.3:c.4989T=	XP_011529155.1:p.Ala1663=
NM_001847.4:c.5022T=	NP_001838.2:p.Ala1674=
NM_033641.4:c.5019T= MANE Select	NP_378667.1:p.Ala1673=
NM_001287758.2:c.5070T=	NP_001274687.1:p.Ala1690=
NM_001287759.2:c.4947T=	NP_001274688.1:p.Ala1649=
NM_001287760.2:c.4848T=	NP_001274689.1:p.Ala1616=