Canonical Allele Identifier: CA359392886

Gene: SLC45A2

Linked Data

• MyVariant Identifiers: chr5:g.33963808A>C (hg19) ; chr5:g.33963703A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33963703A>C , CM000667.2:g.33963703A>C	GRCh38
NC_000005.9:g.33963808A>C , CM000667.1:g.33963808A>C	GRCh37
NC_000005.8:g.33999565A>C	NCBI36
NG_011691.2:g.25973T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.876T>G MANE Select	ENSP00000296589.4:p.Asn292Lys
ENST00000296589.8:c.876T>G	ENSP00000296589.4:p.Asn292Lys
ENST00000382102.7:c.876T>G	ENSP00000371534.3:p.Asn292Lys
ENST00000505056.1:n.678T>G
ENST00000509381.1:c.563-9199T>G	ENSP00000421100.1:n.563-9199T>G
ENST00000510600.1:c.351T>G	ENSP00000424010.1:p.Asn117Lys
NM_001012509.3:c.876T>G	NP_001012527.1:p.Asn292Lys
NM_001297417.2:c.563-9199T>G	NP_001284346.2:n.563-9199T>G
NM_016180.4:c.876T>G	NP_057264.3:p.Asn292Lys
XM_011514051.1:c.474T>G	XP_011512353.1:p.Asn158Lys
XM_011514052.1:c.876T>G	XP_011512354.1:p.Asn292Lys
XR_925620.1:n.1693T>G
NM_016180.5:c.876T>G MANE Select	NP_057264.4:p.Asn292Lys
NM_001012509.4:c.876T>G	NP_001012527.2:p.Asn292Lys
NM_001297417.3:c.563-9199T>G	NP_001284346.2:n.563-9199T>G
NM_001297417.4:c.563-9199T>G	NP_001284346.2:n.563-9199T>G