Canonical Allele Identifier: CA2450721611

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108694911C= , CM000685.2:g.108694911C=	GRCh38
NC_000023.10:g.107938141C= , CM000685.1:g.107938141C=	GRCh37
NC_000023.9:g.107824797C=	NCBI36
NG_011977.1:g.259988C=
NG_011977.2:g.259988C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4811C= MANE Select	ENSP00000331902.7:p.Ser1604=
ENST00000361603.7:c.4793C=	ENSP00000354505.2:p.Ser1598=
ENST00000510690.2:n.1305C=
ENST00000644079.1:n.1297C=
ENST00000328300.10:c.4811C=	ENSP00000331902.6:p.Ser1604=
ENST00000361603.6:c.4793C=	ENSP00000354505.2:p.Ser1598=
ENST00000504541.1:c.209C=	ENSP00000424845.1:p.Ser70=
ENST00000515658.1:c.325-1386C=
NM_000495.4:c.4793C=	NP_000486.1:p.Ser1598=
NM_033380.2:c.4811C=	NP_203699.1:p.Ser1604=
XM_005262070.2:c.4802C=	XP_005262127.1:p.Ser1601=
XM_006724616.2:c.4811C=	XP_006724679.1:p.Ser1604=
XM_011530849.1:c.4487C=	XP_011529151.1:p.Ser1496=
XM_011530851.1:c.2384C=	XP_011529153.1:p.Ser795=
XM_011530849.2:c.4826C=	XP_011529151.2:p.Ser1609=
XM_017029259.2:c.4817C=	XP_016884748.1:p.Ser1606=
XM_017029260.1:c.4808C=	XP_016884749.1:p.Ser1603=
XM_017029263.2:c.3146C=	XP_016884752.1:p.Ser1049=
NM_000495.5:c.4793C=	NP_000486.1:p.Ser1598=
NM_033380.3:c.4811C= MANE Select	NP_203699.1:p.Ser1604=