Canonical Allele Identifier: CA2450541970

Gene: COL4A6

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108157152T= , CM000685.2:g.108157152T=	GRCh38
NC_000023.10:g.107400382T= , CM000685.1:g.107400382T=	GRCh37
NC_000023.9:g.107287038T=	NCBI36
NG_012059.2:g.287323A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334504.12:c.4921A= MANE Select	ENSP00000334733.7:p.Thr1641=
ENST00000334504.11:c.4921A=	ENSP00000334733.7:p.Thr1641=
ENST00000372216.8:c.4924A=	ENSP00000361290.4:p.Thr1642=
ENST00000394872.6:c.4972A=	ENSP00000378340.3:p.Thr1658=
ENST00000538570.5:c.4750A=	ENSP00000445236.1:p.Thr1584=
ENST00000545689.2:c.4885A=	ENSP00000443707.2:p.Thr1629=
ENST00000621266.4:c.4849A=	ENSP00000482970.1:p.Thr1617=
NM_001287758.1:c.4972A=	NP_001274687.1:p.Thr1658=
NM_001287759.1:c.4849A=	NP_001274688.1:p.Thr1617=
NM_001287760.1:c.4750A=	NP_001274689.1:p.Thr1584=
NM_001847.3:c.4924A=	NP_001838.2:p.Thr1642=
NM_033641.3:c.4921A=	NP_378667.1:p.Thr1641=
XM_006724617.2:c.4975A=	XP_006724680.1:p.Thr1659=
XM_011530852.1:c.4903A=	XP_011529154.1:p.Thr1635=
XM_011530853.1:c.4891A=	XP_011529155.1:p.Thr1631=
XM_006724617.3:c.4975A=	XP_006724680.1:p.Thr1659=
XM_011530852.2:c.4903A=	XP_011529154.1:p.Thr1635=
XM_011530853.3:c.4891A=	XP_011529155.1:p.Thr1631=
NM_001847.4:c.4924A=	NP_001838.2:p.Thr1642=
NM_033641.4:c.4921A= MANE Select	NP_378667.1:p.Thr1641=
NM_001287758.2:c.4972A=	NP_001274687.1:p.Thr1658=
NM_001287759.2:c.4849A=	NP_001274688.1:p.Thr1617=
NM_001287760.2:c.4750A=	NP_001274689.1:p.Thr1584=