Canonical Allele Identifier: CA2450721568

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108694809G= , CM000685.2:g.108694809G=	GRCh38
NC_000023.10:g.107938039G= , CM000685.1:g.107938039G=	GRCh37
NC_000023.9:g.107824695G=	NCBI36
NG_011977.1:g.259886G=
NG_011977.2:g.259886G=

Transcript Alleles

HGVS	Amino-acid Change
NM_033380.3:c.4709G= MANE Select	NP_203699.1:p.Cys1570=
ENST00000328300.11:c.4709G= MANE Select	ENSP00000331902.7:p.Cys1570=
NM_000495.4:c.4691G=	NP_000486.1:p.Cys1564=
NM_000495.5:c.4691G=	NP_000486.1:p.Cys1564=
NM_033380.2:c.4709G=	NP_203699.1:p.Cys1570=
ENST00000328300.10:c.4709G=	ENSP00000331902.6:p.Cys1570=
ENST00000361603.6:c.4691G=	ENSP00000354505.2:p.Cys1564=
ENST00000361603.7:c.4691G=	ENSP00000354505.2:p.Cys1564=
ENST00000504541.1:c.107G=	ENSP00000424845.1:p.Cys36=
ENST00000510690.2:n.1203G=
ENST00000515658.1:c.325-1488G=
ENST00000644079.1:n.1195G=
XM_005262070.2:c.4700G=	XP_005262127.1:p.Cys1567=
XM_006724616.2:c.4709G=	XP_006724679.1:p.Cys1570=
XM_011530849.1:c.4385G=	XP_011529151.1:p.Cys1462=
XM_011530849.2:c.4724G=	XP_011529151.2:p.Cys1575=
XM_011530851.1:c.2282G=	XP_011529153.1:p.Cys761=
XM_017029259.2:c.4715G=	XP_016884748.1:p.Cys1572=
XM_017029260.1:c.4706G=	XP_016884749.1:p.Cys1569=
XM_017029263.2:c.3044G=	XP_016884752.1:p.Cys1015=