Canonical Allele Identifier: CA2437508432
Gene: SLC16A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74525756T= , CM000685.2:g.74525756T= GRCh38
NC_000023.10:g.73745591T= , CM000685.1:g.73745591T= GRCh37
NC_000023.9:g.73662316T= NCBI36
NG_011641.1:g.109507T=
NG_011641.2:g.109507T=

Transcript Alleles

HGVS Amino-acid change
ENST00000587091.6:c.1033T= MANE Select ENSP00000465734.1:p.Tyr345=
ENST00000636771.1:c.942T=
ENST00000587091.5:c.1033T= ENSP00000465734.1:p.Tyr345=
ENST00000590447.1:c.473T=
NM_006517.4:c.1033T= NP_006508.2:p.Tyr345=
XM_005262294.1:c.1033T= XP_005262351.1:p.Tyr345=
XM_011531015.1:c.*37T= XP_011529317.1:n.*37T=
NM_006517.5:c.1033T= MANE Select NP_006508.2:p.Tyr345=