Canonical Allele Identifier: CA413905938

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107683392T>A (hg19) ; chrX:g.108440162T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108440162T>A , CM000685.2:g.108440162T>A	GRCh38
NC_000023.10:g.107683392T>A , CM000685.1:g.107683392T>A	GRCh37
NC_000023.9:g.107570048T>A	NCBI36
NG_011977.1:g.5239T>A
NG_012059.2:g.4313A>T
NG_011977.2:g.5239T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.37T>A MANE Select	ENSP00000331902.7:p.Phe13Ile
ENST00000361603.7:c.37T>A	ENSP00000354505.2:p.Phe13Ile
ENST00000642185.1:c.37T>A	ENSP00000495101.1:p.Phe13Ile
ENST00000328300.10:c.37T>A	ENSP00000331902.6:p.Phe13Ile
ENST00000361603.6:c.37T>A	ENSP00000354505.2:p.Phe13Ile
ENST00000470339.1:n.221T>A
ENST00000477429.1:n.319T>A
NM_000495.4:c.37T>A	NP_000486.1:p.Phe13Ile
NM_033380.2:c.37T>A	NP_203699.1:p.Phe13Ile
XM_005262070.2:c.37T>A	XP_005262127.1:p.Phe13Ile
XM_005262072.3:c.37T>A	XP_005262129.1:p.Phe13Ile
XM_006724616.2:c.37T>A	XP_006724679.1:p.Phe13Ile
XM_011530850.1:c.37T>A	XP_011529152.1:p.Phe13Ile
NM_000495.5:c.37T>A	NP_000486.1:p.Phe13Ile
NM_033380.3:c.37T>A MANE Select	NP_203699.1:p.Phe13Ile