Canonical Allele Identifier: CA2765834667
Gene: SLC45A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.33964067_33964068insACA , CM000667.2:g.33964067_33964068insACA GRCh38
NC_000005.9:g.33964172_33964173insACA , CM000667.1:g.33964172_33964173insACA GRCh37
NC_000005.8:g.33999929_33999930insACA NCBI36
NG_011691.2:g.25608_25609insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000296589.9:c.563-52_563-51insTGT MANE Select ENSP00000296589.4:n.563-52_563-51insTGT
ENST00000296589.8:c.563-52_563-51insTGT ENSP00000296589.4:n.563-52_563-51insTGT
ENST00000382102.7:c.563-52_563-51insTGT ENSP00000371534.3:n.563-52_563-51insTGT
ENST00000505056.1:n.365-52_365-51insTGT
ENST00000509381.1:c.563-9564_563-9563insTGT ENSP00000421100.1:n.563-9564_563-9563insTGT
ENST00000510600.1:c.38-52_38-51insTGT ENSP00000424010.1:n.38-52_38-51insTGT
NM_001012509.3:c.563-52_563-51insTGT NP_001012527.1:n.563-52_563-51insTGT
NM_001297417.2:c.563-9564_563-9563insTGT NP_001284346.2:n.563-9564_563-9563insTGT
NM_016180.4:c.563-52_563-51insTGT NP_057264.3:n.563-52_563-51insTGT
XM_011514051.1:c.161-52_161-51insTGT XP_011512353.1:n.161-52_161-51insTGT
XM_011514052.1:c.563-52_563-51insTGT XP_011512354.1:n.563-52_563-51insTGT
XR_925620.1:n.1380-52_1380-51insTGT
NM_016180.5:c.563-52_563-51insTGT MANE Select NP_057264.4:n.563-52_563-51insTGT
NM_001012509.4:c.563-52_563-51insTGT NP_001012527.2:n.563-52_563-51insTGT
NM_001297417.3:c.563-9564_563-9563insTGT NP_001284346.2:n.563-9564_563-9563insTGT
NM_001297417.4:c.563-9564_563-9563insTGT NP_001284346.2:n.563-9564_563-9563insTGT