Canonical Allele Identifier: CA413657837
Gene: SLC16A2 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000587091.6:c.1033T>G MANE Select ENSP00000465734.1:p.Tyr345Asp
ENST00000636771.1:c.942T>G
ENST00000587091.5:c.1033T>G ENSP00000465734.1:p.Tyr345Asp
ENST00000590447.1:c.473T>G
NM_006517.4:c.1033T>G NP_006508.2:p.Tyr345Asp
XM_005262294.1:c.1033T>G XP_005262351.1:p.Tyr345Asp
XM_011531015.1:c.*37T>G XP_011529317.1:n.*37T>G
NM_006517.5:c.1033T>G MANE Select NP_006508.2:p.Tyr345Asp