Canonical Allele Identifier: CA2450722091

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108696377A= , CM000685.2:g.108696377A=	GRCh38
NC_000023.10:g.107939607A= , CM000685.1:g.107939607A=	GRCh37
NC_000023.9:g.107826263A=	NCBI36
NG_011977.1:g.261454A=
NG_011977.2:g.261454A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.5075A= MANE Select	ENSP00000331902.7:p.Ter1692=
ENST00000361603.7:c.5057A=	ENSP00000354505.2:p.Ter1686=
ENST00000510690.2:n.1569A=
ENST00000644079.1:n.2763A=
ENST00000328300.10:c.5075A=	ENSP00000331902.6:p.Ter1692=
ENST00000361603.6:c.5057A=	ENSP00000354505.2:p.Ter1686=
ENST00000504541.1:c.300A=	ENSP00000424845.1:n.300A=
ENST00000515658.1:c.405A=
NM_000495.4:c.5057A=	NP_000486.1:p.Ter1686=
NM_033380.2:c.5075A=	NP_203699.1:p.Ter1692=
XM_005262070.2:c.5066A=	XP_005262127.1:p.Ter1689=
XM_006724616.2:c.5075A=	XP_006724679.1:p.Ter1692=
XM_011530849.1:c.4751A=	XP_011529151.1:p.Ter1584=
XM_011530851.1:c.2648A=	XP_011529153.1:p.Ter883=
XM_011530849.2:c.5090A=	XP_011529151.2:p.Ter1697=
XM_017029259.2:c.5081A=	XP_016884748.1:p.Ter1694=
XM_017029260.1:c.5072A=	XP_016884749.1:p.Ter1691=
XM_017029263.2:c.3410A=	XP_016884752.1:p.Ter1137=
NM_000495.5:c.5057A=	NP_000486.1:p.Ter1686=
NM_033380.3:c.5075A= MANE Select	NP_203699.1:p.Ter1692=