Canonical Allele Identifier: CA2765834740

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33964085_33964086insACA , CM000667.2:g.33964085_33964086insACA	GRCh38
NC_000005.9:g.33964190_33964191insACA , CM000667.1:g.33964190_33964191insACA	GRCh37
NC_000005.8:g.33999947_33999948insACA	NCBI36
NG_011691.2:g.25590_25591insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.563-70_563-69insTGT MANE Select	ENSP00000296589.4:n.563-70_563-69insTGT
ENST00000296589.8:c.563-70_563-69insTGT	ENSP00000296589.4:n.563-70_563-69insTGT
ENST00000382102.7:c.563-70_563-69insTGT	ENSP00000371534.3:n.563-70_563-69insTGT
ENST00000505056.1:n.365-70_365-69insTGT
ENST00000509381.1:c.563-9582_563-9581insTGT	ENSP00000421100.1:n.563-9582_563-9581insTGT
ENST00000510600.1:c.38-70_38-69insTGT	ENSP00000424010.1:n.38-70_38-69insTGT
NM_001012509.3:c.563-70_563-69insTGT	NP_001012527.1:n.563-70_563-69insTGT
NM_001297417.2:c.563-9582_563-9581insTGT	NP_001284346.2:n.563-9582_563-9581insTGT
NM_016180.4:c.563-70_563-69insTGT	NP_057264.3:n.563-70_563-69insTGT
XM_011514051.1:c.161-70_161-69insTGT	XP_011512353.1:n.161-70_161-69insTGT
XM_011514052.1:c.563-70_563-69insTGT	XP_011512354.1:n.563-70_563-69insTGT
XR_925620.1:n.1380-70_1380-69insTGT
NM_016180.5:c.563-70_563-69insTGT MANE Select	NP_057264.4:n.563-70_563-69insTGT
NM_001012509.4:c.563-70_563-69insTGT	NP_001012527.2:n.563-70_563-69insTGT
NM_001297417.3:c.563-9582_563-9581insTGT	NP_001284346.2:n.563-9582_563-9581insTGT
NM_001297417.4:c.563-9582_563-9581insTGT	NP_001284346.2:n.563-9582_563-9581insTGT