Canonical Allele Identifier: CA2450718787

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108686118C= , CM000685.2:g.108686118C=	GRCh38
NC_000023.10:g.107929348C= , CM000685.1:g.107929348C=	GRCh37
NC_000023.9:g.107816004C=	NCBI36
NG_011977.1:g.251195C=
NG_011977.2:g.251195C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4304C= MANE Select	ENSP00000331902.7:p.Pro1435=
ENST00000361603.7:c.4286C=	ENSP00000354505.2:p.Pro1429=
ENST00000510690.2:n.798C=
ENST00000328300.10:c.4304C=	ENSP00000331902.6:p.Pro1435=
ENST00000361603.6:c.4286C=	ENSP00000354505.2:p.Pro1429=
ENST00000489230.1:n.707C=
ENST00000515658.1:c.100C=
NM_000495.4:c.4286C=	NP_000486.1:p.Pro1429=
NM_033380.2:c.4304C=	NP_203699.1:p.Pro1435=
XM_005262070.2:c.4295C=	XP_005262127.1:p.Pro1432=
XM_006724616.2:c.4304C=	XP_006724679.1:p.Pro1435=
XM_011530849.1:c.3980C=	XP_011529151.1:p.Pro1327=
XM_011530851.1:c.1877C=	XP_011529153.1:p.Pro626=
XM_011530849.2:c.4319C=	XP_011529151.2:p.Pro1440=
XM_017029259.2:c.4310C=	XP_016884748.1:p.Pro1437=
XM_017029260.1:c.4301C=	XP_016884749.1:p.Pro1434=
XM_017029263.2:c.2639C=	XP_016884752.1:p.Pro880=
NM_000495.5:c.4286C=	NP_000486.1:p.Pro1429=
NM_033380.3:c.4304C= MANE Select	NP_203699.1:p.Pro1435=