Canonical Allele Identifier: CA2450716921

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108680956G= , CM000685.2:g.108680956G=	GRCh38
NC_000023.10:g.107924186G= , CM000685.1:g.107924186G=	GRCh37
NC_000023.9:g.107810842G=	NCBI36
NG_011977.1:g.246033G=
NG_011977.2:g.246033G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4087G= MANE Select	ENSP00000331902.7:p.Gly1363=
ENST00000361603.7:c.4069G=	ENSP00000354505.2:p.Gly1357=
ENST00000510690.2:n.581G=
ENST00000328300.10:c.4087G=	ENSP00000331902.6:p.Gly1363=
ENST00000361603.6:c.4069G=	ENSP00000354505.2:p.Gly1357=
ENST00000489230.1:n.490G=
NM_000495.4:c.4069G=	NP_000486.1:p.Gly1357=
NM_033380.2:c.4087G=	NP_203699.1:p.Gly1363=
XM_005262070.2:c.4078G=	XP_005262127.1:p.Gly1360=
XM_006724616.2:c.4087G=	XP_006724679.1:p.Gly1363=
XM_011530849.1:c.3763G=	XP_011529151.1:p.Gly1255=
XM_011530851.1:c.1660G=	XP_011529153.1:p.Gly554=
XM_011530849.2:c.4102G=	XP_011529151.2:p.Gly1368=
XM_017029259.2:c.4093G=	XP_016884748.1:p.Gly1365=
XM_017029260.1:c.4084G=	XP_016884749.1:p.Gly1362=
XM_017029263.2:c.2422G=	XP_016884752.1:p.Gly808=
NM_000495.5:c.4069G=	NP_000486.1:p.Gly1357=
NM_033380.3:c.4087G= MANE Select	NP_203699.1:p.Gly1363=