Canonical Allele Identifier: CA2450721599

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108694884G= , CM000685.2:g.108694884G=	GRCh38
NC_000023.10:g.107938114G= , CM000685.1:g.107938114G=	GRCh37
NC_000023.9:g.107824770G=	NCBI36
NG_011977.1:g.259961G=
NG_011977.2:g.259961G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4784G= MANE Select	ENSP00000331902.7:p.Gly1595=
ENST00000361603.7:c.4766G=	ENSP00000354505.2:p.Gly1589=
ENST00000510690.2:n.1278G=
ENST00000644079.1:n.1270G=
ENST00000328300.10:c.4784G=	ENSP00000331902.6:p.Gly1595=
ENST00000361603.6:c.4766G=	ENSP00000354505.2:p.Gly1589=
ENST00000504541.1:c.182G=	ENSP00000424845.1:p.Gly61=
ENST00000515658.1:c.325-1413G=
NM_000495.4:c.4766G=	NP_000486.1:p.Gly1589=
NM_033380.2:c.4784G=	NP_203699.1:p.Gly1595=
XM_005262070.2:c.4775G=	XP_005262127.1:p.Gly1592=
XM_006724616.2:c.4784G=	XP_006724679.1:p.Gly1595=
XM_011530849.1:c.4460G=	XP_011529151.1:p.Gly1487=
XM_011530851.1:c.2357G=	XP_011529153.1:p.Gly786=
XM_011530849.2:c.4799G=	XP_011529151.2:p.Gly1600=
XM_017029259.2:c.4790G=	XP_016884748.1:p.Gly1597=
XM_017029260.1:c.4781G=	XP_016884749.1:p.Gly1594=
XM_017029263.2:c.3119G=	XP_016884752.1:p.Gly1040=
NM_000495.5:c.4766G=	NP_000486.1:p.Gly1589=
NM_033380.3:c.4784G= MANE Select	NP_203699.1:p.Gly1595=