Canonical Allele Identifier: CA116878322

Gene: SLC45A2

Linked Data

• dbSNP Id: rs1008997596
• MyVariant Identifiers: chr5:g.33951938T>G (hg19) ; chr5:g.33951833T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33951833T>G , CM000667.2:g.33951833T>G	GRCh38
NC_000005.9:g.33951938T>G , CM000667.1:g.33951938T>G	GRCh37
NC_000005.8:g.33987695T>G	NCBI36
NG_011691.2:g.37843A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.1033-156A>C MANE Select	ENSP00000296589.4:n.1033-156A>C
ENST00000296589.8:c.1033-156A>C	ENSP00000296589.4:n.1033-156A>C
ENST00000382102.7:c.1033-156A>C	ENSP00000371534.3:n.1033-156A>C
ENST00000509381.1:c.707-156A>C	ENSP00000421100.1:n.707-156A>C
ENST00000510600.1:c.508-156A>C	ENSP00000424010.1:n.508-156A>C
NM_001012509.3:c.1033-156A>C	NP_001012527.1:n.1033-156A>C
NM_001297417.2:c.707-156A>C	NP_001284346.2:n.707-156A>C
NM_016180.4:c.1033-156A>C	NP_057264.3:n.1033-156A>C
XM_011514051.1:c.631-156A>C	XP_011512353.1:n.631-156A>C
XR_925620.1:n.1850-156A>C
NM_016180.5:c.1033-156A>C MANE Select	NP_057264.4:n.1033-156A>C
NM_001012509.4:c.1033-156A>C	NP_001012527.2:n.1033-156A>C
NM_001297417.3:c.707-156A>C	NP_001284346.2:n.707-156A>C
NM_001297417.4:c.707-156A>C	NP_001284346.2:n.707-156A>C