Canonical Allele Identifier: CA2765834821

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33951725_33951726insTG , CM000667.2:g.33951725_33951726insTG	GRCh38
NC_000005.9:g.33951830_33951831insTG , CM000667.1:g.33951830_33951831insTG	GRCh37
NC_000005.8:g.33987587_33987588insTG	NCBI36
NG_011691.2:g.37951_37952insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.1033-48_1033-47insAC MANE Select	ENSP00000296589.4:n.1033-48_1033-47insAC
ENST00000296589.8:c.1033-48_1033-47insAC	ENSP00000296589.4:n.1033-48_1033-47insAC
ENST00000382102.7:c.1033-48_1033-47insAC	ENSP00000371534.3:n.1033-48_1033-47insAC
ENST00000509381.1:c.707-48_707-47insAC	ENSP00000421100.1:n.707-48_707-47insAC
ENST00000510600.1:c.508-48_508-47insAC	ENSP00000424010.1:n.508-48_508-47insAC
NM_001012509.3:c.1033-48_1033-47insAC	NP_001012527.1:n.1033-48_1033-47insAC
NM_001297417.2:c.707-48_707-47insAC	NP_001284346.2:n.707-48_707-47insAC
NM_016180.4:c.1033-48_1033-47insAC	NP_057264.3:n.1033-48_1033-47insAC
XM_011514051.1:c.631-48_631-47insAC	XP_011512353.1:n.631-48_631-47insAC
XR_925620.1:n.1850-48_1850-47insAC
NM_016180.5:c.1033-48_1033-47insAC MANE Select	NP_057264.4:n.1033-48_1033-47insAC
NM_001012509.4:c.1033-48_1033-47insAC	NP_001012527.2:n.1033-48_1033-47insAC
NM_001297417.3:c.707-48_707-47insAC	NP_001284346.2:n.707-48_707-47insAC
NM_001297417.4:c.707-48_707-47insAC	NP_001284346.2:n.707-48_707-47insAC