Canonical Allele Identifier: CA414132390

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107938040T>G (hg19) ; chrX:g.108694810T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108694810T>G , CM000685.2:g.108694810T>G	GRCh38
NC_000023.10:g.107938040T>G , CM000685.1:g.107938040T>G	GRCh37
NC_000023.9:g.107824696T>G	NCBI36
NG_011977.1:g.259887T>G
NG_011977.2:g.259887T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4710T>G MANE Select	ENSP00000331902.7:p.Cys1570Trp
ENST00000361603.7:c.4692T>G	ENSP00000354505.2:p.Cys1564Trp
ENST00000510690.2:n.1204T>G
ENST00000644079.1:n.1196T>G
ENST00000328300.10:c.4710T>G	ENSP00000331902.6:p.Cys1570Trp
ENST00000361603.6:c.4692T>G	ENSP00000354505.2:p.Cys1564Trp
ENST00000504541.1:c.108T>G	ENSP00000424845.1:p.Cys36Trp
ENST00000515658.1:c.325-1487T>G
NM_000495.4:c.4692T>G	NP_000486.1:p.Cys1564Trp
NM_033380.2:c.4710T>G	NP_203699.1:p.Cys1570Trp
XM_005262070.2:c.4701T>G	XP_005262127.1:p.Cys1567Trp
XM_006724616.2:c.4710T>G	XP_006724679.1:p.Cys1570Trp
XM_011530849.1:c.4386T>G	XP_011529151.1:p.Cys1462Trp
XM_011530851.1:c.2283T>G	XP_011529153.1:p.Cys761Trp
XM_011530849.2:c.4725T>G	XP_011529151.2:p.Cys1575Trp
XM_017029259.2:c.4716T>G	XP_016884748.1:p.Cys1572Trp
XM_017029260.1:c.4707T>G	XP_016884749.1:p.Cys1569Trp
XM_017029263.2:c.3045T>G	XP_016884752.1:p.Cys1015Trp
NM_000495.5:c.4692T>G	NP_000486.1:p.Cys1564Trp
NM_033380.3:c.4710T>G MANE Select	NP_203699.1:p.Cys1570Trp