Canonical Allele Identifier: CA2739878531

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33951503T>G , CM000667.2:g.33951503T>G	GRCh38
NC_000005.9:g.33951608T>G , CM000667.1:g.33951608T>G	GRCh37
NC_000005.8:g.33987365T>G	NCBI36
NG_011691.2:g.38173A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000296589.9:c.1156+51A>C MANE Select	ENSP00000296589.4:n.1156+51A>C
ENST00000296589.8:c.1156+51A>C	ENSP00000296589.4:n.1156+51A>C
ENST00000382102.7:c.1156+51A>C	ENSP00000371534.3:n.1156+51A>C
ENST00000509381.1:c.*149A>C	ENSP00000421100.1:n.*149A>C
ENST00000510600.1:c.631+51A>C	ENSP00000424010.1:n.631+51A>C
NM_001012509.3:c.1156+51A>C	NP_001012527.1:n.1156+51A>C
NM_001297417.2:c.*149A>C	NP_001284346.2:n.*149A>C
NM_016180.4:c.1156+51A>C	NP_057264.3:n.1156+51A>C
XM_011514051.1:c.754+51A>C	XP_011512353.1:n.754+51A>C
XR_925620.1:n.1973+51A>C
NM_016180.5:c.1156+51A>C MANE Select	NP_057264.4:n.1156+51A>C
NM_001012509.4:c.1156+51A>C	NP_001012527.2:n.1156+51A>C
NM_001297417.3:c.*149A>C	NP_001284346.2:n.*149A>C
NM_001297417.4:c.*149A>C	NP_001284346.2:n.*149A>C