Canonical Allele Identifier: CA1538211697
Gene: SLC45A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.33951601C= , CM000667.2:g.33951601C= GRCh38
NC_000005.9:g.33951706C= , CM000667.1:g.33951706C= GRCh37
NC_000005.8:g.33987463C= NCBI36
NG_011691.2:g.38075G=

Transcript Alleles

HGVS Amino-acid change
ENST00000296589.9:c.1109G= MANE Select ENSP00000296589.4:p.Gly370=
ENST00000296589.8:c.1109G= ENSP00000296589.4:p.Gly370=
ENST00000382102.7:c.1109G= ENSP00000371534.3:p.Gly370=
ENST00000509381.1:c.*51G= ENSP00000421100.1:n.*51G=
ENST00000510600.1:c.584G= ENSP00000424010.1:p.Gly195=
NM_001012509.3:c.1109G= NP_001012527.1:p.Gly370=
NM_001297417.2:c.*51G= NP_001284346.2:n.*51G=
NM_016180.4:c.1109G= NP_057264.3:p.Gly370=
XM_011514051.1:c.707G= XP_011512353.1:p.Gly236=
XR_925620.1:n.1926G=
NM_016180.5:c.1109G= MANE Select NP_057264.4:p.Gly370=
NM_001012509.4:c.1109G= NP_001012527.2:p.Gly370=
NM_001297417.3:c.*51G= NP_001284346.2:n.*51G=
NM_001297417.4:c.*51G= NP_001284346.2:n.*51G=