Canonical Allele Identifier: CA2765834743

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33964089_33964090del , CM000667.2:g.33964089_33964090del	GRCh38
NC_000005.9:g.33964194_33964195del , CM000667.1:g.33964194_33964195del	GRCh37
NC_000005.8:g.33999951_33999952del	NCBI36
NG_011691.2:g.25588_25589del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.563-72_563-71del MANE Select	ENSP00000296589.4:n.563-72_563-71del
ENST00000296589.8:c.563-72_563-71del	ENSP00000296589.4:n.563-72_563-71del
ENST00000382102.7:c.563-72_563-71del	ENSP00000371534.3:n.563-72_563-71del
ENST00000505056.1:n.365-72_365-71del
ENST00000509381.1:c.563-9584_563-9583del	ENSP00000421100.1:n.563-9584_563-9583del
ENST00000510600.1:c.38-72_38-71del	ENSP00000424010.1:n.38-72_38-71del
NM_001012509.3:c.563-72_563-71del	NP_001012527.1:n.563-72_563-71del
NM_001297417.2:c.563-9584_563-9583del	NP_001284346.2:n.563-9584_563-9583del
NM_016180.4:c.563-72_563-71del	NP_057264.3:n.563-72_563-71del
XM_011514051.1:c.161-72_161-71del	XP_011512353.1:n.161-72_161-71del
XM_011514052.1:c.563-72_563-71del	XP_011512354.1:n.563-72_563-71del
XR_925620.1:n.1380-72_1380-71del
NM_016180.5:c.563-72_563-71del MANE Select	NP_057264.4:n.563-72_563-71del
NM_001012509.4:c.563-72_563-71del	NP_001012527.2:n.563-72_563-71del
NM_001297417.3:c.563-9584_563-9583del	NP_001284346.2:n.563-9584_563-9583del
NM_001297417.4:c.563-9584_563-9583del	NP_001284346.2:n.563-9584_563-9583del