Canonical Allele Identifier: CA1538211652

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33951516_33951517delinsAC , CM000667.2:g.33951516_33951517delinsAC	GRCh38
NC_000005.9:g.33951621_33951622delinsAC , CM000667.1:g.33951621_33951622delinsAC	GRCh37
NC_000005.8:g.33987378_33987379delinsAC	NCBI36
NG_011691.2:g.38159_38160delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.1156+37_1156+38delinsGT MANE Select	ENSP00000296589.4:n.1156+37_1156+38delinsGT
ENST00000296589.8:c.1156+37_1156+38delinsGT	ENSP00000296589.4:n.1156+37_1156+38delinsGT
ENST00000382102.7:c.1156+37_1156+38delinsGT	ENSP00000371534.3:n.1156+37_1156+38delinsGT
ENST00000509381.1:c.*135_*136delinsGT	ENSP00000421100.1:n.*135_*136delinsGT
ENST00000510600.1:c.631+37_631+38delinsGT	ENSP00000424010.1:n.631+37_631+38delinsGT
NM_001012509.3:c.1156+37_1156+38delinsGT	NP_001012527.1:n.1156+37_1156+38delinsGT
NM_001297417.2:c.*135_*136delinsGT	NP_001284346.2:n.*135_*136delinsGT
NM_016180.4:c.1156+37_1156+38delinsGT	NP_057264.3:n.1156+37_1156+38delinsGT
XM_011514051.1:c.754+37_754+38delinsGT	XP_011512353.1:n.754+37_754+38delinsGT
XR_925620.1:n.1973+37_1973+38delinsGT
NM_016180.5:c.1156+37_1156+38delinsGT MANE Select	NP_057264.4:n.1156+37_1156+38delinsGT
NM_001012509.4:c.1156+37_1156+38delinsGT	NP_001012527.2:n.1156+37_1156+38delinsGT
NM_001297417.3:c.*135_*136delinsGT	NP_001284346.2:n.*135_*136delinsGT
NM_001297417.4:c.*135_*136delinsGT	NP_001284346.2:n.*135_*136delinsGT