Canonical Allele Identifier: CA2821813832
Gene: SLC16A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74421760_74421771del , CM000685.2:g.74421760_74421771del GRCh38
NC_000023.10:g.73641595_73641606del , CM000685.1:g.73641595_73641606del GRCh37
NC_000023.9:g.73558320_73558331del NCBI36
NG_011641.1:g.5511_5522del
NG_011641.2:g.5511_5522del

Transcript Alleles

HGVS Amino-acid Change
ENST00000587091.6:c.123_134del MANE Select ENSP00000465734.1:p.Glu42_Pro45del
ENST00000587091.5:c.123_134del ENSP00000465734.1:p.Glu42_Pro45del
NM_006517.4:c.123_134del NP_006508.2:p.Glu42_Pro45del
XM_005262294.1:c.123_134del XP_005262351.1:p.Glu42_Pro45del
XM_011531015.1:c.123_134del XP_011529317.1:p.Glu42_Pro45del
NM_006517.5:c.123_134del MANE Select NP_006508.2:p.Glu42_Pro45del