Canonical Allele Identifier: CA414132580

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107938130G>A (hg19) ; chrX:g.108694900G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108694900G>A , CM000685.2:g.108694900G>A	GRCh38
NC_000023.10:g.107938130G>A , CM000685.1:g.107938130G>A	GRCh37
NC_000023.9:g.107824786G>A	NCBI36
NG_011977.1:g.259977G>A
NG_011977.2:g.259977G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4800G>A MANE Select	ENSP00000331902.7:p.Trp1600Ter
ENST00000361603.7:c.4782G>A	ENSP00000354505.2:p.Trp1594Ter
ENST00000510690.2:n.1294G>A
ENST00000644079.1:n.1286G>A
ENST00000328300.10:c.4800G>A	ENSP00000331902.6:p.Trp1600Ter
ENST00000361603.6:c.4782G>A	ENSP00000354505.2:p.Trp1594Ter
ENST00000504541.1:c.198G>A	ENSP00000424845.1:p.Trp66Ter
ENST00000515658.1:c.325-1397G>A
NM_000495.4:c.4782G>A	NP_000486.1:p.Trp1594Ter
NM_033380.2:c.4800G>A	NP_203699.1:p.Trp1600Ter
XM_005262070.2:c.4791G>A	XP_005262127.1:p.Trp1597Ter
XM_006724616.2:c.4800G>A	XP_006724679.1:p.Trp1600Ter
XM_011530849.1:c.4476G>A	XP_011529151.1:p.Trp1492Ter
XM_011530851.1:c.2373G>A	XP_011529153.1:p.Trp791Ter
XM_011530849.2:c.4815G>A	XP_011529151.2:p.Trp1605Ter
XM_017029259.2:c.4806G>A	XP_016884748.1:p.Trp1602Ter
XM_017029260.1:c.4797G>A	XP_016884749.1:p.Trp1599Ter
XM_017029263.2:c.3135G>A	XP_016884752.1:p.Trp1045Ter
NM_000495.5:c.4782G>A	NP_000486.1:p.Trp1594Ter
NM_033380.3:c.4800G>A MANE Select	NP_203699.1:p.Trp1600Ter