Canonical Allele Identifier: CA1538195633

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33963640_33963641delinsAC , CM000667.2:g.33963640_33963641delinsAC	GRCh38
NC_000005.9:g.33963745_33963746delinsAC , CM000667.1:g.33963745_33963746delinsAC	GRCh37
NC_000005.8:g.33999502_33999503delinsAC	NCBI36
NG_011691.2:g.26035_26036delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.888+50_888+51delinsGT MANE Select	ENSP00000296589.4:n.888+50_888+51delinsGT
ENST00000296589.8:c.888+50_888+51delinsGT	ENSP00000296589.4:n.888+50_888+51delinsGT
ENST00000382102.7:c.888+50_888+51delinsGT	ENSP00000371534.3:n.888+50_888+51delinsGT
ENST00000509381.1:c.563-9137_563-9136delinsGT	ENSP00000421100.1:n.563-9137_563-9136delinsGT
ENST00000510600.1:c.363+50_363+51delinsGT	ENSP00000424010.1:n.363+50_363+51delinsGT
NM_001012509.3:c.888+50_888+51delinsGT	NP_001012527.1:n.888+50_888+51delinsGT
NM_001297417.2:c.563-9137_563-9136delinsGT	NP_001284346.2:n.563-9137_563-9136delinsGT
NM_016180.4:c.888+50_888+51delinsGT	NP_057264.3:n.888+50_888+51delinsGT
XM_011514051.1:c.486+50_486+51delinsGT	XP_011512353.1:n.486+50_486+51delinsGT
XM_011514052.1:c.888+50_888+51delinsGT	XP_011512354.1:n.888+50_888+51delinsGT
XR_925620.1:n.1705+50_1705+51delinsGT
NM_016180.5:c.888+50_888+51delinsGT MANE Select	NP_057264.4:n.888+50_888+51delinsGT
NM_001012509.4:c.888+50_888+51delinsGT	NP_001012527.2:n.888+50_888+51delinsGT
NM_001297417.3:c.563-9137_563-9136delinsGT	NP_001284346.2:n.563-9137_563-9136delinsGT
NM_001297417.4:c.563-9137_563-9136delinsGT	NP_001284346.2:n.563-9137_563-9136delinsGT