Canonical Allele Identifier: CA443659645

Gene: SLC45A2

Linked Data

• dbSNP Id: rs1561364758
• gnomAD v4: 5-33964015-A-T
• MyVariant Identifiers: chr5:g.33964120A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33964015A>T , CM000667.2:g.33964015A>T	GRCh38
NC_000005.9:g.33964120A>T , CM000667.1:g.33964120A>T	GRCh37
NC_000005.8:g.33999877A>T	NCBI36
NG_011691.2:g.25661T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.564T>A MANE Select	ENSP00000296589.4:p.Gly188=
ENST00000296589.8:c.564T>A	ENSP00000296589.4:p.Gly188=
ENST00000382102.7:c.564T>A	ENSP00000371534.3:p.Gly188=
ENST00000505056.1:n.366T>A
ENST00000509381.1:c.563-9511T>A	ENSP00000421100.1:n.563-9511T>A
ENST00000510600.1:c.39T>A	ENSP00000424010.1:p.Gly13=
NM_001012509.3:c.564T>A	NP_001012527.1:p.Gly188=
NM_001297417.2:c.563-9511T>A	NP_001284346.2:n.563-9511T>A
NM_016180.4:c.564T>A	NP_057264.3:p.Gly188=
XM_011514051.1:c.162T>A	XP_011512353.1:p.Gly54=
XM_011514052.1:c.564T>A	XP_011512354.1:p.Gly188=
XR_925620.1:n.1381T>A
NM_016180.5:c.564T>A MANE Select	NP_057264.4:p.Gly188=
NM_001012509.4:c.564T>A	NP_001012527.2:p.Gly188=
NM_001297417.3:c.563-9511T>A	NP_001284346.2:n.563-9511T>A
NM_001297417.4:c.563-9511T>A	NP_001284346.2:n.563-9511T>A