Canonical Allele Identifier: CA517923650

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107924140T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108680910T>G , CM000685.2:g.108680910T>G	GRCh38
NC_000023.10:g.107924140T>G , CM000685.1:g.107924140T>G	GRCh37
NC_000023.9:g.107810796T>G	NCBI36
NG_011977.1:g.245987T>G
NG_011977.2:g.245987T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4041T>G MANE Select	ENSP00000331902.7:p.Pro1347=
ENST00000361603.7:c.4023T>G	ENSP00000354505.2:p.Pro1341=
ENST00000510690.2:n.535T>G
ENST00000328300.10:c.4041T>G	ENSP00000331902.6:p.Pro1347=
ENST00000361603.6:c.4023T>G	ENSP00000354505.2:p.Pro1341=
ENST00000489230.1:n.444T>G
NM_000495.4:c.4023T>G	NP_000486.1:p.Pro1341=
NM_033380.2:c.4041T>G	NP_203699.1:p.Pro1347=
XM_005262070.2:c.4032T>G	XP_005262127.1:p.Pro1344=
XM_006724616.2:c.4041T>G	XP_006724679.1:p.Pro1347=
XM_011530849.1:c.3717T>G	XP_011529151.1:p.Pro1239=
XM_011530851.1:c.1614T>G	XP_011529153.1:p.Pro538=
XM_011530849.2:c.4056T>G	XP_011529151.2:p.Pro1352=
XM_017029259.2:c.4047T>G	XP_016884748.1:p.Pro1349=
XM_017029260.1:c.4038T>G	XP_016884749.1:p.Pro1346=
XM_017029263.2:c.2376T>G	XP_016884752.1:p.Pro792=
NM_000495.5:c.4023T>G	NP_000486.1:p.Pro1341=
NM_033380.3:c.4041T>G MANE Select	NP_203699.1:p.Pro1347=