Canonical Allele Identifier: CA2437472680
Gene: SLC16A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74422047G= , CM000685.2:g.74422047G= GRCh38
NC_000023.10:g.73641882G= , CM000685.1:g.73641882G= GRCh37
NC_000023.9:g.73558607G= NCBI36
NG_011641.1:g.5798G=
NG_011641.2:g.5798G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000587091.6:c.410G= MANE Select ENSP00000465734.1:p.Arg137=
ENST00000636771.1:c.156G=
ENST00000587091.5:c.410G= ENSP00000465734.1:p.Arg137=
NM_006517.4:c.410G= NP_006508.2:p.Arg137=
XM_005262294.1:c.410G= XP_005262351.1:p.Arg137=
XM_011531015.1:c.410G= XP_011529317.1:p.Arg137=
NM_006517.5:c.410G= MANE Select NP_006508.2:p.Arg137=