Canonical Allele Identifier: CA2765834609

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33964037_33964038insAGA , CM000667.2:g.33964037_33964038insAGA	GRCh38
NC_000005.9:g.33964142_33964143insAGA , CM000667.1:g.33964142_33964143insAGA	GRCh37
NC_000005.8:g.33999899_33999900insAGA	NCBI36
NG_011691.2:g.25638_25639insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.563-22_563-21insTCT MANE Select	ENSP00000296589.4:n.563-22_563-21insTCT
ENST00000296589.8:c.563-22_563-21insTCT	ENSP00000296589.4:n.563-22_563-21insTCT
ENST00000382102.7:c.563-22_563-21insTCT	ENSP00000371534.3:n.563-22_563-21insTCT
ENST00000505056.1:n.365-22_365-21insTCT
ENST00000509381.1:c.563-9534_563-9533insTCT	ENSP00000421100.1:n.563-9534_563-9533insTCT
ENST00000510600.1:c.38-22_38-21insTCT	ENSP00000424010.1:n.38-22_38-21insTCT
NM_001012509.3:c.563-22_563-21insTCT	NP_001012527.1:n.563-22_563-21insTCT
NM_001297417.2:c.563-9534_563-9533insTCT	NP_001284346.2:n.563-9534_563-9533insTCT
NM_016180.4:c.563-22_563-21insTCT	NP_057264.3:n.563-22_563-21insTCT
XM_011514051.1:c.161-22_161-21insTCT	XP_011512353.1:n.161-22_161-21insTCT
XM_011514052.1:c.563-22_563-21insTCT	XP_011512354.1:n.563-22_563-21insTCT
XR_925620.1:n.1380-22_1380-21insTCT
NM_016180.5:c.563-22_563-21insTCT MANE Select	NP_057264.4:n.563-22_563-21insTCT
NM_001012509.4:c.563-22_563-21insTCT	NP_001012527.2:n.563-22_563-21insTCT
NM_001297417.3:c.563-9534_563-9533insTCT	NP_001284346.2:n.563-9534_563-9533insTCT
NM_001297417.4:c.563-9534_563-9533insTCT	NP_001284346.2:n.563-9534_563-9533insTCT