Canonical Allele Identifier: CA2765834706

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33964076_33964077insA , CM000667.2:g.33964076_33964077insA	GRCh38
NC_000005.9:g.33964181_33964182insA , CM000667.1:g.33964181_33964182insA	GRCh37
NC_000005.8:g.33999938_33999939insA	NCBI36
NG_011691.2:g.25599_25600insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.563-61_563-60insT MANE Select	ENSP00000296589.4:n.563-61_563-60insT
ENST00000296589.8:c.563-61_563-60insT	ENSP00000296589.4:n.563-61_563-60insT
ENST00000382102.7:c.563-61_563-60insT	ENSP00000371534.3:n.563-61_563-60insT
ENST00000505056.1:n.365-61_365-60insT
ENST00000509381.1:c.563-9573_563-9572insT	ENSP00000421100.1:n.563-9573_563-9572insT
ENST00000510600.1:c.38-61_38-60insT	ENSP00000424010.1:n.38-61_38-60insT
NM_001012509.3:c.563-61_563-60insT	NP_001012527.1:n.563-61_563-60insT
NM_001297417.2:c.563-9573_563-9572insT	NP_001284346.2:n.563-9573_563-9572insT
NM_016180.4:c.563-61_563-60insT	NP_057264.3:n.563-61_563-60insT
XM_011514051.1:c.161-61_161-60insT	XP_011512353.1:n.161-61_161-60insT
XM_011514052.1:c.563-61_563-60insT	XP_011512354.1:n.563-61_563-60insT
XR_925620.1:n.1380-61_1380-60insT
NM_016180.5:c.563-61_563-60insT MANE Select	NP_057264.4:n.563-61_563-60insT
NM_001012509.4:c.563-61_563-60insT	NP_001012527.2:n.563-61_563-60insT
NM_001297417.3:c.563-9573_563-9572insT	NP_001284346.2:n.563-9573_563-9572insT
NM_001297417.4:c.563-9573_563-9572insT	NP_001284346.2:n.563-9573_563-9572insT