Canonical Allele Identifier: CA1538211724
Gene: SLC45A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.33951651A= , CM000667.2:g.33951651A= GRCh38
NC_000005.9:g.33951756A= , CM000667.1:g.33951756A= GRCh37
NC_000005.8:g.33987513A= NCBI36
NG_011691.2:g.38025T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296589.9:c.1059T= MANE Select ENSP00000296589.4:p.Ser353=
ENST00000296589.8:c.1059T= ENSP00000296589.4:p.Ser353=
ENST00000382102.7:c.1059T= ENSP00000371534.3:p.Ser353=
ENST00000509381.1:c.*1T= ENSP00000421100.1:n.*1T=
ENST00000510600.1:c.534T= ENSP00000424010.1:p.Ser178=
NM_001012509.3:c.1059T= NP_001012527.1:p.Ser353=
NM_001297417.2:c.*1T= NP_001284346.2:n.*1T=
NM_016180.4:c.1059T= NP_057264.3:p.Ser353=
XM_011514051.1:c.657T= XP_011512353.1:p.Ser219=
XR_925620.1:n.1876T=
NM_016180.5:c.1059T= MANE Select NP_057264.4:p.Ser353=
NM_001012509.4:c.1059T= NP_001012527.2:p.Ser353=
NM_001297417.3:c.*1T= NP_001284346.2:n.*1T=
NM_001297417.4:c.*1T= NP_001284346.2:n.*1T=