Canonical Allele Identifier: CA2450542002

Gene: COL4A6

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108157257T= , CM000685.2:g.108157257T=	GRCh38
NC_000023.10:g.107400487T= , CM000685.1:g.107400487T=	GRCh37
NC_000023.9:g.107287143T=	NCBI36
NG_012059.2:g.287218A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334504.12:c.4816A= MANE Select	ENSP00000334733.7:p.Thr1606=
ENST00000334504.11:c.4816A=	ENSP00000334733.7:p.Thr1606=
ENST00000372216.8:c.4819A=	ENSP00000361290.4:p.Thr1607=
ENST00000394872.6:c.4867A=	ENSP00000378340.3:p.Thr1623=
ENST00000538570.5:c.4645A=	ENSP00000445236.1:p.Thr1549=
ENST00000545689.2:c.4780A=	ENSP00000443707.2:p.Thr1594=
ENST00000621266.4:c.4744A=	ENSP00000482970.1:p.Thr1582=
NM_001287758.1:c.4867A=	NP_001274687.1:p.Thr1623=
NM_001287759.1:c.4744A=	NP_001274688.1:p.Thr1582=
NM_001287760.1:c.4645A=	NP_001274689.1:p.Thr1549=
NM_001847.3:c.4819A=	NP_001838.2:p.Thr1607=
NM_033641.3:c.4816A=	NP_378667.1:p.Thr1606=
XM_006724617.2:c.4870A=	XP_006724680.1:p.Thr1624=
XM_011530852.1:c.4798A=	XP_011529154.1:p.Thr1600=
XM_011530853.1:c.4786A=	XP_011529155.1:p.Thr1596=
XM_006724617.3:c.4870A=	XP_006724680.1:p.Thr1624=
XM_011530852.2:c.4798A=	XP_011529154.1:p.Thr1600=
XM_011530853.3:c.4786A=	XP_011529155.1:p.Thr1596=
NM_001847.4:c.4819A=	NP_001838.2:p.Thr1607=
NM_033641.4:c.4816A= MANE Select	NP_378667.1:p.Thr1606=
NM_001287758.2:c.4867A=	NP_001274687.1:p.Thr1623=
NM_001287759.2:c.4744A=	NP_001274688.1:p.Thr1582=
NM_001287760.2:c.4645A=	NP_001274689.1:p.Thr1549=