Canonical Allele Identifier: CA413658047
Gene: SLC16A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74525851C>A , CM000685.2:g.74525851C>A GRCh38
NC_000023.10:g.73745686C>A , CM000685.1:g.73745686C>A GRCh37
NC_000023.9:g.73662411C>A NCBI36
NG_011641.1:g.109602C>A
NG_011641.2:g.109602C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000587091.6:c.1128C>A MANE Select ENSP00000465734.1:p.His376Gln
ENST00000636771.1:c.1037C>A
ENST00000587091.5:c.1128C>A ENSP00000465734.1:p.His376Gln
ENST00000590447.1:c.568C>A
NM_006517.4:c.1128C>A NP_006508.2:p.His376Gln
XM_005262294.1:c.1128C>A XP_005262351.1:p.His376Gln
NM_006517.5:c.1128C>A MANE Select NP_006508.2:p.His376Gln