Canonical Allele Identifier: CA2765834922

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33951827_33951828insACA , CM000667.2:g.33951827_33951828insACA	GRCh38
NC_000005.9:g.33951932_33951933insACA , CM000667.1:g.33951932_33951933insACA	GRCh37
NC_000005.8:g.33987689_33987690insACA	NCBI36
NG_011691.2:g.37848_37849insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.1033-151_1033-150insTGT MANE Select	ENSP00000296589.4:n.1033-151_1033-150insTGT
ENST00000296589.8:c.1033-151_1033-150insTGT	ENSP00000296589.4:n.1033-151_1033-150insTGT
ENST00000382102.7:c.1033-151_1033-150insTGT	ENSP00000371534.3:n.1033-151_1033-150insTGT
ENST00000509381.1:c.707-151_707-150insTGT	ENSP00000421100.1:n.707-151_707-150insTGT
ENST00000510600.1:c.508-151_508-150insTGT	ENSP00000424010.1:n.508-151_508-150insTGT
NM_001012509.3:c.1033-151_1033-150insTGT	NP_001012527.1:n.1033-151_1033-150insTGT
NM_001297417.2:c.707-151_707-150insTGT	NP_001284346.2:n.707-151_707-150insTGT
NM_016180.4:c.1033-151_1033-150insTGT	NP_057264.3:n.1033-151_1033-150insTGT
XM_011514051.1:c.631-151_631-150insTGT	XP_011512353.1:n.631-151_631-150insTGT
XR_925620.1:n.1850-151_1850-150insTGT
NM_016180.5:c.1033-151_1033-150insTGT MANE Select	NP_057264.4:n.1033-151_1033-150insTGT
NM_001012509.4:c.1033-151_1033-150insTGT	NP_001012527.2:n.1033-151_1033-150insTGT
NM_001297417.3:c.707-151_707-150insTGT	NP_001284346.2:n.707-151_707-150insTGT
NM_001297417.4:c.707-151_707-150insTGT	NP_001284346.2:n.707-151_707-150insTGT