Canonical Allele Identifier: CA2765834637

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33964060C>A , CM000667.2:g.33964060C>A	GRCh38
NC_000005.9:g.33964165C>A , CM000667.1:g.33964165C>A	GRCh37
NC_000005.8:g.33999922C>A	NCBI36
NG_011691.2:g.25616G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.563-44G>T MANE Select	ENSP00000296589.4:n.563-44G>T
ENST00000296589.8:c.563-44G>T	ENSP00000296589.4:n.563-44G>T
ENST00000382102.7:c.563-44G>T	ENSP00000371534.3:n.563-44G>T
ENST00000505056.1:n.365-44G>T
ENST00000509381.1:c.563-9556G>T	ENSP00000421100.1:n.563-9556G>T
ENST00000510600.1:c.38-44G>T	ENSP00000424010.1:n.38-44G>T
NM_001012509.3:c.563-44G>T	NP_001012527.1:n.563-44G>T
NM_001297417.2:c.563-9556G>T	NP_001284346.2:n.563-9556G>T
NM_016180.4:c.563-44G>T	NP_057264.3:n.563-44G>T
XM_011514051.1:c.161-44G>T	XP_011512353.1:n.161-44G>T
XM_011514052.1:c.563-44G>T	XP_011512354.1:n.563-44G>T
XR_925620.1:n.1380-44G>T
NM_016180.5:c.563-44G>T MANE Select	NP_057264.4:n.563-44G>T
NM_001012509.4:c.563-44G>T	NP_001012527.2:n.563-44G>T
NM_001297417.3:c.563-9556G>T	NP_001284346.2:n.563-9556G>T
NM_001297417.4:c.563-9556G>T	NP_001284346.2:n.563-9556G>T