Canonical Allele Identifier: CA2437472632
Gene: SLC16A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74421894G= , CM000685.2:g.74421894G= GRCh38
NC_000023.10:g.73641729G= , CM000685.1:g.73641729G= GRCh37
NC_000023.9:g.73558454G= NCBI36
NG_011641.1:g.5645G=
NG_011641.2:g.5645G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000587091.6:c.257G= MANE Select ENSP00000465734.1:p.Arg86=
ENST00000636771.1:c.3G=
ENST00000587091.5:c.257G= ENSP00000465734.1:p.Arg86=
NM_006517.4:c.257G= NP_006508.2:p.Arg86=
XM_005262294.1:c.257G= XP_005262351.1:p.Arg86=
XM_011531015.1:c.257G= XP_011529317.1:p.Arg86=
NM_006517.5:c.257G= MANE Select NP_006508.2:p.Arg86=