Canonical Allele Identifier: CA1538218586
Gene: SLC45A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.33984428C= , CM000667.2:g.33984428C= GRCh38
NC_000005.9:g.33984533C= , CM000667.1:g.33984533C= GRCh37
NC_000005.8:g.34020290C= NCBI36
NG_011691.2:g.5248G=

Transcript Alleles

HGVS Amino-acid change
ENST00000296589.9:c.156G= MANE Select ENSP00000296589.4:p.Glu52=
ENST00000296589.8:c.156G= ENSP00000296589.4:p.Glu52=
ENST00000382102.7:c.156G= ENSP00000371534.3:p.Glu52=
ENST00000505056.1:n.135G=
ENST00000509381.1:c.156G= ENSP00000421100.1:p.Glu52=
NM_001012509.3:c.156G= NP_001012527.1:p.Glu52=
NM_001297417.2:c.156G= NP_001284346.2:p.Glu52=
NM_016180.4:c.156G= NP_057264.3:p.Glu52=
XM_011514052.1:c.156G= XP_011512354.1:p.Glu52=
XR_925620.1:n.717G=
NM_016180.5:c.156G= MANE Select NP_057264.4:p.Glu52=
NM_001012509.4:c.156G= NP_001012527.2:p.Glu52=
NM_001297417.3:c.156G= NP_001284346.2:p.Glu52=
NM_001297417.4:c.156G= NP_001284346.2:p.Glu52=