Canonical Allele Identifier: CA2765834655

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33964062_33964063insAG , CM000667.2:g.33964062_33964063insAG	GRCh38
NC_000005.9:g.33964167_33964168insAG , CM000667.1:g.33964167_33964168insAG	GRCh37
NC_000005.8:g.33999924_33999925insAG	NCBI36
NG_011691.2:g.25613_25614insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.563-47_563-46insCT MANE Select	ENSP00000296589.4:n.563-47_563-46insCT
ENST00000296589.8:c.563-47_563-46insCT	ENSP00000296589.4:n.563-47_563-46insCT
ENST00000382102.7:c.563-47_563-46insCT	ENSP00000371534.3:n.563-47_563-46insCT
ENST00000505056.1:n.365-47_365-46insCT
ENST00000509381.1:c.563-9559_563-9558insCT	ENSP00000421100.1:n.563-9559_563-9558insCT
ENST00000510600.1:c.38-47_38-46insCT	ENSP00000424010.1:n.38-47_38-46insCT
NM_001012509.3:c.563-47_563-46insCT	NP_001012527.1:n.563-47_563-46insCT
NM_001297417.2:c.563-9559_563-9558insCT	NP_001284346.2:n.563-9559_563-9558insCT
NM_016180.4:c.563-47_563-46insCT	NP_057264.3:n.563-47_563-46insCT
XM_011514051.1:c.161-47_161-46insCT	XP_011512353.1:n.161-47_161-46insCT
XM_011514052.1:c.563-47_563-46insCT	XP_011512354.1:n.563-47_563-46insCT
XR_925620.1:n.1380-47_1380-46insCT
NM_016180.5:c.563-47_563-46insCT MANE Select	NP_057264.4:n.563-47_563-46insCT
NM_001012509.4:c.563-47_563-46insCT	NP_001012527.2:n.563-47_563-46insCT
NM_001297417.3:c.563-9559_563-9558insCT	NP_001284346.2:n.563-9559_563-9558insCT
NM_001297417.4:c.563-9559_563-9558insCT	NP_001284346.2:n.563-9559_563-9558insCT