Canonical Allele Identifier: CA2450719262

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108687555T= , CM000685.2:g.108687555T=	GRCh38
NC_000023.10:g.107930785T= , CM000685.1:g.107930785T=	GRCh37
NC_000023.9:g.107817441T=	NCBI36
NG_011977.1:g.252632T=
NG_011977.2:g.252632T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000328300.11:c.4389T= MANE Select	ENSP00000331902.7:p.Ser1463=
ENST00000361603.7:c.4371T=	ENSP00000354505.2:p.Ser1457=
ENST00000510690.2:n.883T=
ENST00000328300.10:c.4389T=	ENSP00000331902.6:p.Ser1463=
ENST00000361603.6:c.4371T=	ENSP00000354505.2:p.Ser1457=
ENST00000515658.1:c.185T=
NM_000495.4:c.4371T=	NP_000486.1:p.Ser1457=
NM_033380.2:c.4389T=	NP_203699.1:p.Ser1463=
XM_005262070.2:c.4380T=	XP_005262127.1:p.Ser1460=
XM_006724616.2:c.4389T=	XP_006724679.1:p.Ser1463=
XM_011530849.1:c.4065T=	XP_011529151.1:p.Ser1355=
XM_011530851.1:c.1962T=	XP_011529153.1:p.Ser654=
XM_011530849.2:c.4404T=	XP_011529151.2:p.Ser1468=
XM_017029259.2:c.4395T=	XP_016884748.1:p.Ser1465=
XM_017029260.1:c.4386T=	XP_016884749.1:p.Ser1462=
XM_017029263.2:c.2724T=	XP_016884752.1:p.Ser908=
NM_000495.5:c.4371T=	NP_000486.1:p.Ser1457=
NM_033380.3:c.4389T= MANE Select	NP_203699.1:p.Ser1463=