Canonical Allele Identifier: CA413854622

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107930874T>A (hg19) ; chrX:g.108687644T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108687644T>A , CM000685.2:g.108687644T>A	GRCh38
NC_000023.10:g.107930874T>A , CM000685.1:g.107930874T>A	GRCh37
NC_000023.9:g.107817530T>A	NCBI36
NG_011977.1:g.252721T>A
NG_011977.2:g.252721T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4478T>A MANE Select	ENSP00000331902.7:p.Phe1493Tyr
ENST00000361603.7:c.4460T>A	ENSP00000354505.2:p.Phe1487Tyr
ENST00000510690.2:n.972T>A
ENST00000328300.10:c.4478T>A	ENSP00000331902.6:p.Phe1493Tyr
ENST00000361603.6:c.4460T>A	ENSP00000354505.2:p.Phe1487Tyr
ENST00000515658.1:c.274T>A
NM_000495.4:c.4460T>A	NP_000486.1:p.Phe1487Tyr
NM_033380.2:c.4478T>A	NP_203699.1:p.Phe1493Tyr
XM_005262070.2:c.4469T>A	XP_005262127.1:p.Phe1490Tyr
XM_006724616.2:c.4478T>A	XP_006724679.1:p.Phe1493Tyr
XM_011530849.1:c.4154T>A	XP_011529151.1:p.Phe1385Tyr
XM_011530851.1:c.2051T>A	XP_011529153.1:p.Phe684Tyr
XM_011530849.2:c.4493T>A	XP_011529151.2:p.Phe1498Tyr
XM_017029259.2:c.4484T>A	XP_016884748.1:p.Phe1495Tyr
XM_017029260.1:c.4475T>A	XP_016884749.1:p.Phe1492Tyr
XM_017029263.2:c.2813T>A	XP_016884752.1:p.Phe938Tyr
NM_000495.5:c.4460T>A	NP_000486.1:p.Phe1487Tyr
NM_033380.3:c.4478T>A MANE Select	NP_203699.1:p.Phe1493Tyr