Canonical Allele Identifier: CA359392828

Gene: SLC45A2

Linked Data

• MyVariant Identifiers: chr5:g.33963797T>C (hg19) ; chr5:g.33963692T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33963692T>C , CM000667.2:g.33963692T>C	GRCh38
NC_000005.9:g.33963797T>C , CM000667.1:g.33963797T>C	GRCh37
NC_000005.8:g.33999554T>C	NCBI36
NG_011691.2:g.25984A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.887A>G MANE Select	ENSP00000296589.4:p.Gln296Arg
ENST00000296589.8:c.887A>G	ENSP00000296589.4:p.Gln296Arg
ENST00000382102.7:c.887A>G	ENSP00000371534.3:p.Gln296Arg
ENST00000505056.1:n.689A>G
ENST00000509381.1:c.563-9188A>G	ENSP00000421100.1:n.563-9188A>G
ENST00000510600.1:c.362A>G	ENSP00000424010.1:p.Gln121Arg
NM_001012509.3:c.887A>G	NP_001012527.1:p.Gln296Arg
NM_001297417.2:c.563-9188A>G	NP_001284346.2:n.563-9188A>G
NM_016180.4:c.887A>G	NP_057264.3:p.Gln296Arg
XM_011514051.1:c.485A>G	XP_011512353.1:p.Gln162Arg
XM_011514052.1:c.887A>G	XP_011512354.1:p.Gln296Arg
XR_925620.1:n.1704A>G
NM_016180.5:c.887A>G MANE Select	NP_057264.4:p.Gln296Arg
NM_001012509.4:c.887A>G	NP_001012527.2:p.Gln296Arg
NM_001297417.3:c.563-9188A>G	NP_001284346.2:n.563-9188A>G
NM_001297417.4:c.563-9188A>G	NP_001284346.2:n.563-9188A>G