Canonical Allele Identifier: CA2450719257

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108687550T= , CM000685.2:g.108687550T=	GRCh38
NC_000023.10:g.107930780T= , CM000685.1:g.107930780T=	GRCh37
NC_000023.9:g.107817436T=	NCBI36
NG_011977.1:g.252627T=
NG_011977.2:g.252627T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000328300.11:c.4384T= MANE Select	ENSP00000331902.7:p.Ser1462=
ENST00000361603.7:c.4366T=	ENSP00000354505.2:p.Ser1456=
ENST00000510690.2:n.878T=
ENST00000328300.10:c.4384T=	ENSP00000331902.6:p.Ser1462=
ENST00000361603.6:c.4366T=	ENSP00000354505.2:p.Ser1456=
ENST00000515658.1:c.180T=
NM_000495.4:c.4366T=	NP_000486.1:p.Ser1456=
NM_033380.2:c.4384T=	NP_203699.1:p.Ser1462=
XM_005262070.2:c.4375T=	XP_005262127.1:p.Ser1459=
XM_006724616.2:c.4384T=	XP_006724679.1:p.Ser1462=
XM_011530849.1:c.4060T=	XP_011529151.1:p.Ser1354=
XM_011530851.1:c.1957T=	XP_011529153.1:p.Ser653=
XM_011530849.2:c.4399T=	XP_011529151.2:p.Ser1467=
XM_017029259.2:c.4390T=	XP_016884748.1:p.Ser1464=
XM_017029260.1:c.4381T=	XP_016884749.1:p.Ser1461=
XM_017029263.2:c.2719T=	XP_016884752.1:p.Ser907=
NM_000495.5:c.4366T=	NP_000486.1:p.Ser1456=
NM_033380.3:c.4384T= MANE Select	NP_203699.1:p.Ser1462=