Canonical Allele Identifier: CA2450716909

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108680934A= , CM000685.2:g.108680934A=	GRCh38
NC_000023.10:g.107924164A= , CM000685.1:g.107924164A=	GRCh37
NC_000023.9:g.107810820A=	NCBI36
NG_011977.1:g.246011A=
NG_011977.2:g.246011A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4065A= MANE Select	ENSP00000331902.7:p.Glu1355=
ENST00000361603.7:c.4047A=	ENSP00000354505.2:p.Glu1349=
ENST00000510690.2:n.559A=
ENST00000328300.10:c.4065A=	ENSP00000331902.6:p.Glu1355=
ENST00000361603.6:c.4047A=	ENSP00000354505.2:p.Glu1349=
ENST00000489230.1:n.468A=
NM_000495.4:c.4047A=	NP_000486.1:p.Glu1349=
NM_033380.2:c.4065A=	NP_203699.1:p.Glu1355=
XM_005262070.2:c.4056A=	XP_005262127.1:p.Glu1352=
XM_006724616.2:c.4065A=	XP_006724679.1:p.Glu1355=
XM_011530849.1:c.3741A=	XP_011529151.1:p.Glu1247=
XM_011530851.1:c.1638A=	XP_011529153.1:p.Glu546=
XM_011530849.2:c.4080A=	XP_011529151.2:p.Glu1360=
XM_017029259.2:c.4071A=	XP_016884748.1:p.Glu1357=
XM_017029260.1:c.4062A=	XP_016884749.1:p.Glu1354=
XM_017029263.2:c.2400A=	XP_016884752.1:p.Glu800=
NM_000495.5:c.4047A=	NP_000486.1:p.Glu1349=
NM_033380.3:c.4065A= MANE Select	NP_203699.1:p.Glu1355=