Canonical Allele Identifier: CA2450719245

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108687535G= , CM000685.2:g.108687535G=	GRCh38
NC_000023.10:g.107930765G= , CM000685.1:g.107930765G=	GRCh37
NC_000023.9:g.107817421G=	NCBI36
NG_011977.1:g.252612G=
NG_011977.2:g.252612G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000328300.11:c.4369G= MANE Select	ENSP00000331902.7:p.Gly1457=
ENST00000361603.7:c.4351G=	ENSP00000354505.2:p.Gly1451=
ENST00000510690.2:n.863G=
ENST00000328300.10:c.4369G=	ENSP00000331902.6:p.Gly1457=
ENST00000361603.6:c.4351G=	ENSP00000354505.2:p.Gly1451=
ENST00000515658.1:c.165G=
NM_000495.4:c.4351G=	NP_000486.1:p.Gly1451=
NM_033380.2:c.4369G=	NP_203699.1:p.Gly1457=
XM_005262070.2:c.4360G=	XP_005262127.1:p.Gly1454=
XM_006724616.2:c.4369G=	XP_006724679.1:p.Gly1457=
XM_011530849.1:c.4045G=	XP_011529151.1:p.Gly1349=
XM_011530851.1:c.1942G=	XP_011529153.1:p.Gly648=
XM_011530849.2:c.4384G=	XP_011529151.2:p.Gly1462=
XM_017029259.2:c.4375G=	XP_016884748.1:p.Gly1459=
XM_017029260.1:c.4366G=	XP_016884749.1:p.Gly1456=
XM_017029263.2:c.2704G=	XP_016884752.1:p.Gly902=
NM_000495.5:c.4351G=	NP_000486.1:p.Gly1451=
NM_033380.3:c.4369G= MANE Select	NP_203699.1:p.Gly1457=