Canonical Allele Identifier: CA1538211712
Gene: SLC45A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.33951628A= , CM000667.2:g.33951628A= GRCh38
NC_000005.9:g.33951733A= , CM000667.1:g.33951733A= GRCh37
NC_000005.8:g.33987490A= NCBI36
NG_011691.2:g.38048T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296589.9:c.1082T= MANE Select ENSP00000296589.4:p.Leu361=
ENST00000296589.8:c.1082T= ENSP00000296589.4:p.Leu361=
ENST00000382102.7:c.1082T= ENSP00000371534.3:p.Leu361=
ENST00000509381.1:c.*24T= ENSP00000421100.1:n.*24T=
ENST00000510600.1:c.557T= ENSP00000424010.1:p.Leu186=
NM_001012509.3:c.1082T= NP_001012527.1:p.Leu361=
NM_001297417.2:c.*24T= NP_001284346.2:n.*24T=
NM_016180.4:c.1082T= NP_057264.3:p.Leu361=
XM_011514051.1:c.680T= XP_011512353.1:p.Leu227=
XR_925620.1:n.1899T=
NM_016180.5:c.1082T= MANE Select NP_057264.4:p.Leu361=
NM_001012509.4:c.1082T= NP_001012527.2:p.Leu361=
NM_001297417.3:c.*24T= NP_001284346.2:n.*24T=
NM_001297417.4:c.*24T= NP_001284346.2:n.*24T=