Canonical Allele Identifier: CA2765834866

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33951769_33951770insAGA , CM000667.2:g.33951769_33951770insAGA	GRCh38
NC_000005.9:g.33951874_33951875insAGA , CM000667.1:g.33951874_33951875insAGA	GRCh37
NC_000005.8:g.33987631_33987632insAGA	NCBI36
NG_011691.2:g.37906_37907insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.1033-93_1033-92insTCT MANE Select	ENSP00000296589.4:n.1033-93_1033-92insTCT
ENST00000296589.8:c.1033-93_1033-92insTCT	ENSP00000296589.4:n.1033-93_1033-92insTCT
ENST00000382102.7:c.1033-93_1033-92insTCT	ENSP00000371534.3:n.1033-93_1033-92insTCT
ENST00000509381.1:c.707-93_707-92insTCT	ENSP00000421100.1:n.707-93_707-92insTCT
ENST00000510600.1:c.508-93_508-92insTCT	ENSP00000424010.1:n.508-93_508-92insTCT
NM_001012509.3:c.1033-93_1033-92insTCT	NP_001012527.1:n.1033-93_1033-92insTCT
NM_001297417.2:c.707-93_707-92insTCT	NP_001284346.2:n.707-93_707-92insTCT
NM_016180.4:c.1033-93_1033-92insTCT	NP_057264.3:n.1033-93_1033-92insTCT
XM_011514051.1:c.631-93_631-92insTCT	XP_011512353.1:n.631-93_631-92insTCT
XR_925620.1:n.1850-93_1850-92insTCT
NM_016180.5:c.1033-93_1033-92insTCT MANE Select	NP_057264.4:n.1033-93_1033-92insTCT
NM_001012509.4:c.1033-93_1033-92insTCT	NP_001012527.2:n.1033-93_1033-92insTCT
NM_001297417.3:c.707-93_707-92insTCT	NP_001284346.2:n.707-93_707-92insTCT
NM_001297417.4:c.707-93_707-92insTCT	NP_001284346.2:n.707-93_707-92insTCT