Canonical Allele Identifier: CA2450721596

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108694874T= , CM000685.2:g.108694874T=	GRCh38
NC_000023.10:g.107938104T= , CM000685.1:g.107938104T=	GRCh37
NC_000023.9:g.107824760T=	NCBI36
NG_011977.1:g.259951T=
NG_011977.2:g.259951T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4774T= MANE Select	ENSP00000331902.7:p.Cys1592=
ENST00000361603.7:c.4756T=	ENSP00000354505.2:p.Cys1586=
ENST00000510690.2:n.1268T=
ENST00000644079.1:n.1260T=
ENST00000328300.10:c.4774T=	ENSP00000331902.6:p.Cys1592=
ENST00000361603.6:c.4756T=	ENSP00000354505.2:p.Cys1586=
ENST00000504541.1:c.172T=	ENSP00000424845.1:p.Cys58=
ENST00000515658.1:c.325-1423T=
NM_000495.4:c.4756T=	NP_000486.1:p.Cys1586=
NM_033380.2:c.4774T=	NP_203699.1:p.Cys1592=
XM_005262070.2:c.4765T=	XP_005262127.1:p.Cys1589=
XM_006724616.2:c.4774T=	XP_006724679.1:p.Cys1592=
XM_011530849.1:c.4450T=	XP_011529151.1:p.Cys1484=
XM_011530851.1:c.2347T=	XP_011529153.1:p.Cys783=
XM_011530849.2:c.4789T=	XP_011529151.2:p.Cys1597=
XM_017029259.2:c.4780T=	XP_016884748.1:p.Cys1594=
XM_017029260.1:c.4771T=	XP_016884749.1:p.Cys1591=
XM_017029263.2:c.3109T=	XP_016884752.1:p.Cys1037=
NM_000495.5:c.4756T=	NP_000486.1:p.Cys1586=
NM_033380.3:c.4774T= MANE Select	NP_203699.1:p.Cys1592=