Canonical Allele Identifier: CA413658035
Gene: SLC16A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74525846G>A , CM000685.2:g.74525846G>A GRCh38
NC_000023.10:g.73745681G>A , CM000685.1:g.73745681G>A GRCh37
NC_000023.9:g.73662406G>A NCBI36
NG_011641.1:g.109597G>A
NG_011641.2:g.109597G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000587091.6:c.1123G>A MANE Select ENSP00000465734.1:p.Gly375Ser
ENST00000636771.1:c.1032G>A
ENST00000587091.5:c.1123G>A ENSP00000465734.1:p.Gly375Ser
ENST00000590447.1:c.563G>A
NM_006517.4:c.1123G>A NP_006508.2:p.Gly375Ser
XM_005262294.1:c.1123G>A XP_005262351.1:p.Gly375Ser
NM_006517.5:c.1123G>A MANE Select NP_006508.2:p.Gly375Ser