Canonical Allele Identifier: CA2450719255

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108687548C= , CM000685.2:g.108687548C=	GRCh38
NC_000023.10:g.107930778C= , CM000685.1:g.107930778C=	GRCh37
NC_000023.9:g.107817434C=	NCBI36
NG_011977.1:g.252625C=
NG_011977.2:g.252625C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4382C= MANE Select	ENSP00000331902.7:p.Thr1461=
ENST00000361603.7:c.4364C=	ENSP00000354505.2:p.Thr1455=
ENST00000510690.2:n.876C=
ENST00000328300.10:c.4382C=	ENSP00000331902.6:p.Thr1461=
ENST00000361603.6:c.4364C=	ENSP00000354505.2:p.Thr1455=
ENST00000515658.1:c.178C=
NM_000495.4:c.4364C=	NP_000486.1:p.Thr1455=
NM_033380.2:c.4382C=	NP_203699.1:p.Thr1461=
XM_005262070.2:c.4373C=	XP_005262127.1:p.Thr1458=
XM_006724616.2:c.4382C=	XP_006724679.1:p.Thr1461=
XM_011530849.1:c.4058C=	XP_011529151.1:p.Thr1353=
XM_011530851.1:c.1955C=	XP_011529153.1:p.Thr652=
XM_011530849.2:c.4397C=	XP_011529151.2:p.Thr1466=
XM_017029259.2:c.4388C=	XP_016884748.1:p.Thr1463=
XM_017029260.1:c.4379C=	XP_016884749.1:p.Thr1460=
XM_017029263.2:c.2717C=	XP_016884752.1:p.Thr906=
NM_000495.5:c.4364C=	NP_000486.1:p.Thr1455=
NM_033380.3:c.4382C= MANE Select	NP_203699.1:p.Thr1461=