Canonical Allele Identifier: CA413657835
Gene: SLC16A2 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000587091.6:c.1033T>A MANE Select ENSP00000465734.1:p.Tyr345Asn
ENST00000636771.1:c.942T>A
ENST00000587091.5:c.1033T>A ENSP00000465734.1:p.Tyr345Asn
ENST00000590447.1:c.473T>A
NM_006517.4:c.1033T>A NP_006508.2:p.Tyr345Asn
XM_005262294.1:c.1033T>A XP_005262351.1:p.Tyr345Asn
XM_011531015.1:c.*37T>A XP_011529317.1:n.*37T>A
NM_006517.5:c.1033T>A MANE Select NP_006508.2:p.Tyr345Asn