Canonical Allele Identifier: CA2437508454
Gene: SLC16A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74525854C= , CM000685.2:g.74525854C= GRCh38
NC_000023.10:g.73745689C= , CM000685.1:g.73745689C= GRCh37
NC_000023.9:g.73662414C= NCBI36
NG_011641.1:g.109605C=
NG_011641.2:g.109605C=

Transcript Alleles

HGVS Amino-acid change
ENST00000587091.6:c.1131C= MANE Select ENSP00000465734.1:p.Ile377=
ENST00000636771.1:c.1040C=
ENST00000587091.5:c.1131C= ENSP00000465734.1:p.Ile377=
ENST00000590447.1:c.571C=
NM_006517.4:c.1131C= NP_006508.2:p.Ile377=
XM_005262294.1:c.1131C= XP_005262351.1:p.Ile377=
NM_006517.5:c.1131C= MANE Select NP_006508.2:p.Ile377=