Canonical Allele Identifier: CA414133162

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107939589T>G (hg19) ; chrX:g.108696359T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108696359T>G , CM000685.2:g.108696359T>G	GRCh38
NC_000023.10:g.107939589T>G , CM000685.1:g.107939589T>G	GRCh37
NC_000023.9:g.107826245T>G	NCBI36
NG_011977.1:g.261436T>G
NG_011977.2:g.261436T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.5057T>G MANE Select	ENSP00000331902.7:p.Val1686Gly
ENST00000361603.7:c.5039T>G	ENSP00000354505.2:p.Val1680Gly
ENST00000510690.2:n.1551T>G
ENST00000644079.1:n.2745T>G
ENST00000328300.10:c.5057T>G	ENSP00000331902.6:p.Val1686Gly
ENST00000361603.6:c.5039T>G	ENSP00000354505.2:p.Val1680Gly
ENST00000504541.1:c.282T>G	ENSP00000424845.1:n.282T>G
ENST00000515658.1:c.387T>G
NM_000495.4:c.5039T>G	NP_000486.1:p.Val1680Gly
NM_033380.2:c.5057T>G	NP_203699.1:p.Val1686Gly
XM_005262070.2:c.5048T>G	XP_005262127.1:p.Val1683Gly
XM_006724616.2:c.5057T>G	XP_006724679.1:p.Val1686Gly
XM_011530849.1:c.4733T>G	XP_011529151.1:p.Val1578Gly
XM_011530851.1:c.2630T>G	XP_011529153.1:p.Val877Gly
XM_011530849.2:c.5072T>G	XP_011529151.2:p.Val1691Gly
XM_017029259.2:c.5063T>G	XP_016884748.1:p.Val1688Gly
XM_017029260.1:c.5054T>G	XP_016884749.1:p.Val1685Gly
XM_017029263.2:c.3392T>G	XP_016884752.1:p.Val1131Gly
NM_000495.5:c.5039T>G	NP_000486.1:p.Val1680Gly
NM_033380.3:c.5057T>G MANE Select	NP_203699.1:p.Val1686Gly