Canonical Allele Identifier: CA2450551431

Gene: COL4A6

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108187279C= , CM000685.2:g.108187279C=	GRCh38
NC_000023.10:g.107430509C= , CM000685.1:g.107430509C=	GRCh37
NC_000023.9:g.107317165C=	NCBI36
NG_012059.2:g.257196G=

Transcript Alleles

HGVS	Amino-acid Change
NM_033641.4:c.1768G= MANE Select	NP_378667.1:p.Gly590=
ENST00000334504.12:c.1768G= MANE Select	ENSP00000334733.7:p.Gly590=
NM_001287758.1:c.1768G=	NP_001274687.1:p.Gly590=
NM_001287758.2:c.1768G=	NP_001274687.1:p.Gly590=
NM_001287759.1:c.1768G=	NP_001274688.1:p.Gly590=
NM_001287759.2:c.1768G=	NP_001274688.1:p.Gly590=
NM_001287760.1:c.1768G=	NP_001274689.1:p.Gly590=
NM_001287760.2:c.1768G=	NP_001274689.1:p.Gly590=
NM_001847.3:c.1771G=	NP_001838.2:p.Gly591=
NM_001847.4:c.1771G=	NP_001838.2:p.Gly591=
NM_033641.3:c.1768G=	NP_378667.1:p.Gly590=
ENST00000334504.11:c.1768G=	ENSP00000334733.7:p.Gly590=
ENST00000372216.8:c.1771G=	ENSP00000361290.4:p.Gly591=
ENST00000394872.6:c.1768G=	ENSP00000378340.3:p.Gly590=
ENST00000538570.5:c.1768G=	ENSP00000445236.1:p.Gly590=
ENST00000545689.2:c.1768G=	ENSP00000443707.2:p.Gly590=
ENST00000621266.4:c.1768G=	ENSP00000482970.1:p.Gly590=
XM_006724617.2:c.1771G=	XP_006724680.1:p.Gly591=
XM_006724617.3:c.1771G=	XP_006724680.1:p.Gly591=
XM_011530852.1:c.1771G=	XP_011529154.1:p.Gly591=
XM_011530852.2:c.1771G=	XP_011529154.1:p.Gly591=
XM_011530853.1:c.1687G=	XP_011529155.1:p.Gly563=
XM_011530853.3:c.1687G=	XP_011529155.1:p.Gly563=
XM_011530854.1:c.1771G=	XP_011529156.1:p.Gly591=
XM_011530854.2:c.1771G=	XP_011529156.1:p.Gly591=
XR_001755650.1:n.1893G=