Canonical Allele Identifier: CA1538195613

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33963628_33963629delinsAC , CM000667.2:g.33963628_33963629delinsAC	GRCh38
NC_000005.9:g.33963733_33963734delinsAC , CM000667.1:g.33963733_33963734delinsAC	GRCh37
NC_000005.8:g.33999490_33999491delinsAC	NCBI36
NG_011691.2:g.26047_26048delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.888+62_888+63delinsGT MANE Select	ENSP00000296589.4:n.888+62_888+63delinsGT
ENST00000296589.8:c.888+62_888+63delinsGT	ENSP00000296589.4:n.888+62_888+63delinsGT
ENST00000382102.7:c.888+62_888+63delinsGT	ENSP00000371534.3:n.888+62_888+63delinsGT
ENST00000509381.1:c.563-9125_563-9124delinsGT	ENSP00000421100.1:n.563-9125_563-9124delinsGT
ENST00000510600.1:c.363+62_363+63delinsGT	ENSP00000424010.1:n.363+62_363+63delinsGT
NM_001012509.3:c.888+62_888+63delinsGT	NP_001012527.1:n.888+62_888+63delinsGT
NM_001297417.2:c.563-9125_563-9124delinsGT	NP_001284346.2:n.563-9125_563-9124delinsGT
NM_016180.4:c.888+62_888+63delinsGT	NP_057264.3:n.888+62_888+63delinsGT
XM_011514051.1:c.486+62_486+63delinsGT	XP_011512353.1:n.486+62_486+63delinsGT
XM_011514052.1:c.888+62_888+63delinsGT	XP_011512354.1:n.888+62_888+63delinsGT
XR_925620.1:n.1705+62_1705+63delinsGT
NM_016180.5:c.888+62_888+63delinsGT MANE Select	NP_057264.4:n.888+62_888+63delinsGT
NM_001012509.4:c.888+62_888+63delinsGT	NP_001012527.2:n.888+62_888+63delinsGT
NM_001297417.3:c.563-9125_563-9124delinsGT	NP_001284346.2:n.563-9125_563-9124delinsGT
NM_001297417.4:c.563-9125_563-9124delinsGT	NP_001284346.2:n.563-9125_563-9124delinsGT