Canonical Allele Identifier: CA2695234517
Gene: SLC16A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74525752dup , CM000685.2:g.74525752dup GRCh38
NC_000023.10:g.73745587dup , CM000685.1:g.73745587dup GRCh37
NC_000023.9:g.73662312dup NCBI36
NG_011641.1:g.109503dup
NG_011641.2:g.109503dup

Transcript Alleles

HGVS Amino-acid change
ENST00000587091.6:c.1029dup MANE Select ENSP00000465734.1:p.Lys344GlufsTer?
ENST00000636771.1:c.938dup
ENST00000587091.5:c.1029dup ENSP00000465734.1:p.Lys344GlufsTer?
ENST00000590447.1:c.469dup
NM_006517.4:c.1029dup NP_006508.2:p.Lys344GlufsTer?
XM_005262294.1:c.1029dup XP_005262351.1:p.Lys344GlufsTer?
XM_011531015.1:c.*33dup XP_011529317.1:n.*33dup
NM_006517.5:c.1029dup MANE Select NP_006508.2:p.Lys344GlufsTer?