Canonical Allele Identifier: CA517923844

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107925066C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108681836C>A , CM000685.2:g.108681836C>A	GRCh38
NC_000023.10:g.107925066C>A , CM000685.1:g.107925066C>A	GRCh37
NC_000023.9:g.107811722C>A	NCBI36
NG_011977.1:g.246913C>A
NG_011977.2:g.246913C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000328300.11:c.4164C>A MANE Select	ENSP00000331902.7:p.Gly1388=
ENST00000361603.7:c.4146C>A	ENSP00000354505.2:p.Gly1382=
ENST00000510690.2:n.658C>A
ENST00000328300.10:c.4164C>A	ENSP00000331902.6:p.Gly1388=
ENST00000361603.6:c.4146C>A	ENSP00000354505.2:p.Gly1382=
ENST00000489230.1:n.567C>A
NM_000495.4:c.4146C>A	NP_000486.1:p.Gly1382=
NM_033380.2:c.4164C>A	NP_203699.1:p.Gly1388=
XM_005262070.2:c.4155C>A	XP_005262127.1:p.Gly1385=
XM_006724616.2:c.4164C>A	XP_006724679.1:p.Gly1388=
XM_011530849.1:c.3840C>A	XP_011529151.1:p.Gly1280=
XM_011530851.1:c.1737C>A	XP_011529153.1:p.Gly579=
XM_011530849.2:c.4179C>A	XP_011529151.2:p.Gly1393=
XM_017029259.2:c.4170C>A	XP_016884748.1:p.Gly1390=
XM_017029260.1:c.4161C>A	XP_016884749.1:p.Gly1387=
XM_017029263.2:c.2499C>A	XP_016884752.1:p.Gly833=
NM_000495.5:c.4146C>A	NP_000486.1:p.Gly1382=
NM_033380.3:c.4164C>A MANE Select	NP_203699.1:p.Gly1388=