Canonical Allele Identifier: CA2840544943
Gene: SLC16A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74421948dup , CM000685.2:g.74421948dup GRCh38
NC_000023.10:g.73641783dup , CM000685.1:g.73641783dup GRCh37
NC_000023.9:g.73558508dup NCBI36
NG_011641.1:g.5699dup
NG_011641.2:g.5699dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000587091.6:c.311dup MANE Select ENSP00000465734.1:p.Phe105ValfsTer15
ENST00000636771.1:c.57dup
ENST00000587091.5:c.311dup ENSP00000465734.1:p.Phe105ValfsTer15
NM_006517.4:c.311dup NP_006508.2:p.Phe105ValfsTer15
XM_005262294.1:c.311dup XP_005262351.1:p.Phe105ValfsTer15
XM_011531015.1:c.311dup XP_011529317.1:p.Phe105ValfsTer15
NM_006517.5:c.311dup MANE Select NP_006508.2:p.Phe105ValfsTer15