Canonical Allele Identifier: CA2765834625

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33964051_33964052insACA , CM000667.2:g.33964051_33964052insACA	GRCh38
NC_000005.9:g.33964156_33964157insACA , CM000667.1:g.33964156_33964157insACA	GRCh37
NC_000005.8:g.33999913_33999914insACA	NCBI36
NG_011691.2:g.25624_25625insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.563-36_563-35insTGT MANE Select	ENSP00000296589.4:n.563-36_563-35insTGT
ENST00000296589.8:c.563-36_563-35insTGT	ENSP00000296589.4:n.563-36_563-35insTGT
ENST00000382102.7:c.563-36_563-35insTGT	ENSP00000371534.3:n.563-36_563-35insTGT
ENST00000505056.1:n.365-36_365-35insTGT
ENST00000509381.1:c.563-9548_563-9547insTGT	ENSP00000421100.1:n.563-9548_563-9547insTGT
ENST00000510600.1:c.38-36_38-35insTGT	ENSP00000424010.1:n.38-36_38-35insTGT
NM_001012509.3:c.563-36_563-35insTGT	NP_001012527.1:n.563-36_563-35insTGT
NM_001297417.2:c.563-9548_563-9547insTGT	NP_001284346.2:n.563-9548_563-9547insTGT
NM_016180.4:c.563-36_563-35insTGT	NP_057264.3:n.563-36_563-35insTGT
XM_011514051.1:c.161-36_161-35insTGT	XP_011512353.1:n.161-36_161-35insTGT
XM_011514052.1:c.563-36_563-35insTGT	XP_011512354.1:n.563-36_563-35insTGT
XR_925620.1:n.1380-36_1380-35insTGT
NM_016180.5:c.563-36_563-35insTGT MANE Select	NP_057264.4:n.563-36_563-35insTGT
NM_001012509.4:c.563-36_563-35insTGT	NP_001012527.2:n.563-36_563-35insTGT
NM_001297417.3:c.563-9548_563-9547insTGT	NP_001284346.2:n.563-9548_563-9547insTGT
NM_001297417.4:c.563-9548_563-9547insTGT	NP_001284346.2:n.563-9548_563-9547insTGT