Canonical Allele Identifier: CA414132980

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107938654T>A (hg19) ; chrX:g.108695424T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108695424T>A , CM000685.2:g.108695424T>A	GRCh38
NC_000023.10:g.107938654T>A , CM000685.1:g.107938654T>A	GRCh37
NC_000023.9:g.107825310T>A	NCBI36
NG_011977.1:g.260501T>A
NG_011977.2:g.260501T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4979T>A MANE Select	ENSP00000331902.7:p.Val1660Glu
ENST00000361603.7:c.4961T>A	ENSP00000354505.2:p.Val1654Glu
ENST00000510690.2:n.1473T>A
ENST00000644079.1:n.1810T>A
ENST00000328300.10:c.4979T>A	ENSP00000331902.6:p.Val1660Glu
ENST00000361603.6:c.4961T>A	ENSP00000354505.2:p.Val1654Glu
ENST00000504541.1:c.219+503T>A	ENSP00000424845.1:n.219+503T>A
ENST00000515658.1:c.325-873T>A
NM_000495.4:c.4961T>A	NP_000486.1:p.Val1654Glu
NM_033380.2:c.4979T>A	NP_203699.1:p.Val1660Glu
XM_005262070.2:c.4970T>A	XP_005262127.1:p.Val1657Glu
XM_006724616.2:c.4979T>A	XP_006724679.1:p.Val1660Glu
XM_011530849.1:c.4655T>A	XP_011529151.1:p.Val1552Glu
XM_011530851.1:c.2552T>A	XP_011529153.1:p.Val851Glu
XM_011530849.2:c.4994T>A	XP_011529151.2:p.Val1665Glu
XM_017029259.2:c.4985T>A	XP_016884748.1:p.Val1662Glu
XM_017029260.1:c.4976T>A	XP_016884749.1:p.Val1659Glu
XM_017029263.2:c.3314T>A	XP_016884752.1:p.Val1105Glu
NM_000495.5:c.4961T>A	NP_000486.1:p.Val1654Glu
NM_033380.3:c.4979T>A MANE Select	NP_203699.1:p.Val1660Glu