Canonical Allele Identifier: CA2765834921

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33951826_33951827insAGA , CM000667.2:g.33951826_33951827insAGA	GRCh38
NC_000005.9:g.33951931_33951932insAGA , CM000667.1:g.33951931_33951932insAGA	GRCh37
NC_000005.8:g.33987688_33987689insAGA	NCBI36
NG_011691.2:g.37849_37850insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.1033-150_1033-149insTCT MANE Select	ENSP00000296589.4:n.1033-150_1033-149insTCT
ENST00000296589.8:c.1033-150_1033-149insTCT	ENSP00000296589.4:n.1033-150_1033-149insTCT
ENST00000382102.7:c.1033-150_1033-149insTCT	ENSP00000371534.3:n.1033-150_1033-149insTCT
ENST00000509381.1:c.707-150_707-149insTCT	ENSP00000421100.1:n.707-150_707-149insTCT
ENST00000510600.1:c.508-150_508-149insTCT	ENSP00000424010.1:n.508-150_508-149insTCT
NM_001012509.3:c.1033-150_1033-149insTCT	NP_001012527.1:n.1033-150_1033-149insTCT
NM_001297417.2:c.707-150_707-149insTCT	NP_001284346.2:n.707-150_707-149insTCT
NM_016180.4:c.1033-150_1033-149insTCT	NP_057264.3:n.1033-150_1033-149insTCT
XM_011514051.1:c.631-150_631-149insTCT	XP_011512353.1:n.631-150_631-149insTCT
XR_925620.1:n.1850-150_1850-149insTCT
NM_016180.5:c.1033-150_1033-149insTCT MANE Select	NP_057264.4:n.1033-150_1033-149insTCT
NM_001012509.4:c.1033-150_1033-149insTCT	NP_001012527.2:n.1033-150_1033-149insTCT
NM_001297417.3:c.707-150_707-149insTCT	NP_001284346.2:n.707-150_707-149insTCT
NM_001297417.4:c.707-150_707-149insTCT	NP_001284346.2:n.707-150_707-149insTCT