Canonical Allele Identifier: CA2765834669

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33964068_33964069insAGA , CM000667.2:g.33964068_33964069insAGA	GRCh38
NC_000005.9:g.33964173_33964174insAGA , CM000667.1:g.33964173_33964174insAGA	GRCh37
NC_000005.8:g.33999930_33999931insAGA	NCBI36
NG_011691.2:g.25607_25608insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.563-53_563-52insTCT MANE Select	ENSP00000296589.4:n.563-53_563-52insTCT
ENST00000296589.8:c.563-53_563-52insTCT	ENSP00000296589.4:n.563-53_563-52insTCT
ENST00000382102.7:c.563-53_563-52insTCT	ENSP00000371534.3:n.563-53_563-52insTCT
ENST00000505056.1:n.365-53_365-52insTCT
ENST00000509381.1:c.563-9565_563-9564insTCT	ENSP00000421100.1:n.563-9565_563-9564insTCT
ENST00000510600.1:c.38-53_38-52insTCT	ENSP00000424010.1:n.38-53_38-52insTCT
NM_001012509.3:c.563-53_563-52insTCT	NP_001012527.1:n.563-53_563-52insTCT
NM_001297417.2:c.563-9565_563-9564insTCT	NP_001284346.2:n.563-9565_563-9564insTCT
NM_016180.4:c.563-53_563-52insTCT	NP_057264.3:n.563-53_563-52insTCT
XM_011514051.1:c.161-53_161-52insTCT	XP_011512353.1:n.161-53_161-52insTCT
XM_011514052.1:c.563-53_563-52insTCT	XP_011512354.1:n.563-53_563-52insTCT
XR_925620.1:n.1380-53_1380-52insTCT
NM_016180.5:c.563-53_563-52insTCT MANE Select	NP_057264.4:n.563-53_563-52insTCT
NM_001012509.4:c.563-53_563-52insTCT	NP_001012527.2:n.563-53_563-52insTCT
NM_001297417.3:c.563-9565_563-9564insTCT	NP_001284346.2:n.563-9565_563-9564insTCT
NM_001297417.4:c.563-9565_563-9564insTCT	NP_001284346.2:n.563-9565_563-9564insTCT