Canonical Allele Identifier: CA1538211707
Gene: SLC45A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.33951621G= , CM000667.2:g.33951621G= GRCh38
NC_000005.9:g.33951726G= , CM000667.1:g.33951726G= GRCh37
NC_000005.8:g.33987483G= NCBI36
NG_011691.2:g.38055C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296589.9:c.1089C= MANE Select ENSP00000296589.4:p.Tyr363=
ENST00000296589.8:c.1089C= ENSP00000296589.4:p.Tyr363=
ENST00000382102.7:c.1089C= ENSP00000371534.3:p.Tyr363=
ENST00000509381.1:c.*31C= ENSP00000421100.1:n.*31C=
ENST00000510600.1:c.564C= ENSP00000424010.1:p.Tyr188=
NM_001012509.3:c.1089C= NP_001012527.1:p.Tyr363=
NM_001297417.2:c.*31C= NP_001284346.2:n.*31C=
NM_016180.4:c.1089C= NP_057264.3:p.Tyr363=
XM_011514051.1:c.687C= XP_011512353.1:p.Tyr229=
XR_925620.1:n.1906C=
NM_016180.5:c.1089C= MANE Select NP_057264.4:p.Tyr363=
NM_001012509.4:c.1089C= NP_001012527.2:p.Tyr363=
NM_001297417.3:c.*31C= NP_001284346.2:n.*31C=
NM_001297417.4:c.*31C= NP_001284346.2:n.*31C=