Canonical Allele Identifier: CA2450688826

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108598758C= , CM000685.2:g.108598758C=	GRCh38
NC_000023.10:g.107841988C= , CM000685.1:g.107841988C=	GRCh37
NC_000023.9:g.107728644C=	NCBI36
NG_011977.1:g.163835C=
NG_011977.2:g.163835C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000328300.11:c.1836C= MANE Select	ENSP00000331902.7:p.Gly612=
ENST00000361603.7:c.1836C=	ENSP00000354505.2:p.Gly612=
ENST00000328300.10:c.1836C=	ENSP00000331902.6:p.Gly612=
ENST00000361603.6:c.1836C=	ENSP00000354505.2:p.Gly612=
ENST00000483338.1:n.1292C=
NM_000495.4:c.1836C=	NP_000486.1:p.Gly612=
NM_033380.2:c.1836C=	NP_203699.1:p.Gly612=
XM_005262070.2:c.1836C=	XP_005262127.1:p.Gly612=
XM_005262072.3:c.1836C=	XP_005262129.1:p.Gly612=
XM_006724616.2:c.1836C=	XP_006724679.1:p.Gly612=
XM_011530849.1:c.1512C=	XP_011529151.1:p.Gly504=
XM_011530850.1:c.1836C=	XP_011529152.1:p.Gly612=
XM_011530849.2:c.1851C=	XP_011529151.2:p.Gly617=
XM_017029259.2:c.1851C=	XP_016884748.1:p.Gly617=
XM_017029260.1:c.1851C=	XP_016884749.1:p.Gly617=
XM_017029261.1:c.1851C=	XP_016884750.1:p.Gly617=
XM_017029262.2:c.1851C=	XP_016884751.1:p.Gly617=
XM_017029263.2:c.171C=	XP_016884752.1:p.Gly57=
NM_000495.5:c.1836C=	NP_000486.1:p.Gly612=
NM_033380.3:c.1836C= MANE Select	NP_203699.1:p.Gly612=