Canonical Allele Identifier: CA2695234497
Gene: SLC16A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74421922dup , CM000685.2:g.74421922dup GRCh38
NC_000023.10:g.73641757dup , CM000685.1:g.73641757dup GRCh37
NC_000023.9:g.73558482dup NCBI36
NG_011641.1:g.5673dup
NG_011641.2:g.5673dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000587091.6:c.285dup MANE Select ENSP00000465734.1:p.Glu96ArgfsTer24
ENST00000636771.1:c.31dup
ENST00000587091.5:c.285dup ENSP00000465734.1:p.Glu96ArgfsTer24
NM_006517.4:c.285dup NP_006508.2:p.Glu96ArgfsTer24
XM_005262294.1:c.285dup XP_005262351.1:p.Glu96ArgfsTer24
XM_011531015.1:c.285dup XP_011529317.1:p.Glu96ArgfsTer24
NM_006517.5:c.285dup MANE Select NP_006508.2:p.Glu96ArgfsTer24