Canonical Allele Identifier: CA1538195574

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33963621_33963624delinsTAAA , CM000667.2:g.33963621_33963624delinsTAAA	GRCh38
NC_000005.9:g.33963726_33963729delinsTAAA , CM000667.1:g.33963726_33963729delinsTAAA	GRCh37
NC_000005.8:g.33999483_33999486delinsTAAA	NCBI36
NG_011691.2:g.26052_26055delinsTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.888+67_888+70delinsTTTA MANE Select	ENSP00000296589.4:n.888+67_888+70delinsTTTA
ENST00000296589.8:c.888+67_888+70delinsTTTA	ENSP00000296589.4:n.888+67_888+70delinsTTTA
ENST00000382102.7:c.888+67_888+70delinsTTTA	ENSP00000371534.3:n.888+67_888+70delinsTTTA
ENST00000509381.1:c.563-9120_563-9117delinsTTTA	ENSP00000421100.1:n.563-9120_563-9117delinsTTTA
ENST00000510600.1:c.363+67_363+70delinsTTTA	ENSP00000424010.1:n.363+67_363+70delinsTTTA
NM_001012509.3:c.888+67_888+70delinsTTTA	NP_001012527.1:n.888+67_888+70delinsTTTA
NM_001297417.2:c.563-9120_563-9117delinsTTTA	NP_001284346.2:n.563-9120_563-9117delinsTTTA
NM_016180.4:c.888+67_888+70delinsTTTA	NP_057264.3:n.888+67_888+70delinsTTTA
XM_011514051.1:c.486+67_486+70delinsTTTA	XP_011512353.1:n.486+67_486+70delinsTTTA
XM_011514052.1:c.888+67_888+70delinsTTTA	XP_011512354.1:n.888+67_888+70delinsTTTA
XR_925620.1:n.1705+67_1705+70delinsTTTA
NM_016180.5:c.888+67_888+70delinsTTTA MANE Select	NP_057264.4:n.888+67_888+70delinsTTTA
NM_001012509.4:c.888+67_888+70delinsTTTA	NP_001012527.2:n.888+67_888+70delinsTTTA
NM_001297417.3:c.563-9120_563-9117delinsTTTA	NP_001284346.2:n.563-9120_563-9117delinsTTTA
NM_001297417.4:c.563-9120_563-9117delinsTTTA	NP_001284346.2:n.563-9120_563-9117delinsTTTA