Canonical Allele Identifier: CA359394398

Gene: SLC45A2

Linked Data

• MyVariant Identifiers: chr5:g.33964116C>G (hg19) ; chr5:g.33964011C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33964011C>G , CM000667.2:g.33964011C>G	GRCh38
NC_000005.9:g.33964116C>G , CM000667.1:g.33964116C>G	GRCh37
NC_000005.8:g.33999873C>G	NCBI36
NG_011691.2:g.25665G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.568G>C MANE Select	ENSP00000296589.4:p.Gly190Arg
ENST00000296589.8:c.568G>C	ENSP00000296589.4:p.Gly190Arg
ENST00000382102.7:c.568G>C	ENSP00000371534.3:p.Gly190Arg
ENST00000505056.1:n.370G>C
ENST00000509381.1:c.563-9507G>C	ENSP00000421100.1:n.563-9507G>C
ENST00000510600.1:c.43G>C	ENSP00000424010.1:p.Gly15Arg
NM_001012509.3:c.568G>C	NP_001012527.1:p.Gly190Arg
NM_001297417.2:c.563-9507G>C	NP_001284346.2:n.563-9507G>C
NM_016180.4:c.568G>C	NP_057264.3:p.Gly190Arg
XM_011514051.1:c.166G>C	XP_011512353.1:p.Gly56Arg
XM_011514052.1:c.568G>C	XP_011512354.1:p.Gly190Arg
XR_925620.1:n.1385G>C
NM_016180.5:c.568G>C MANE Select	NP_057264.4:p.Gly190Arg
NM_001012509.4:c.568G>C	NP_001012527.2:p.Gly190Arg
NM_001297417.3:c.563-9507G>C	NP_001284346.2:n.563-9507G>C
NM_001297417.4:c.563-9507G>C	NP_001284346.2:n.563-9507G>C