Canonical Allele Identifier: CA414132604

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107938143T>A (hg19) ; chrX:g.108694913T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108694913T>A , CM000685.2:g.108694913T>A	GRCh38
NC_000023.10:g.107938143T>A , CM000685.1:g.107938143T>A	GRCh37
NC_000023.9:g.107824799T>A	NCBI36
NG_011977.1:g.259990T>A
NG_011977.2:g.259990T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4813T>A MANE Select	ENSP00000331902.7:p.Phe1605Ile
ENST00000361603.7:c.4795T>A	ENSP00000354505.2:p.Phe1599Ile
ENST00000510690.2:n.1307T>A
ENST00000644079.1:n.1299T>A
ENST00000328300.10:c.4813T>A	ENSP00000331902.6:p.Phe1605Ile
ENST00000361603.6:c.4795T>A	ENSP00000354505.2:p.Phe1599Ile
ENST00000504541.1:c.211T>A	ENSP00000424845.1:p.Phe71Ile
ENST00000515658.1:c.325-1384T>A
NM_000495.4:c.4795T>A	NP_000486.1:p.Phe1599Ile
NM_033380.2:c.4813T>A	NP_203699.1:p.Phe1605Ile
XM_005262070.2:c.4804T>A	XP_005262127.1:p.Phe1602Ile
XM_006724616.2:c.4813T>A	XP_006724679.1:p.Phe1605Ile
XM_011530849.1:c.4489T>A	XP_011529151.1:p.Phe1497Ile
XM_011530851.1:c.2386T>A	XP_011529153.1:p.Phe796Ile
XM_011530849.2:c.4828T>A	XP_011529151.2:p.Phe1610Ile
XM_017029259.2:c.4819T>A	XP_016884748.1:p.Phe1607Ile
XM_017029260.1:c.4810T>A	XP_016884749.1:p.Phe1604Ile
XM_017029263.2:c.3148T>A	XP_016884752.1:p.Phe1050Ile
NM_000495.5:c.4795T>A	NP_000486.1:p.Phe1599Ile
NM_033380.3:c.4813T>A MANE Select	NP_203699.1:p.Phe1605Ile