Canonical Allele Identifier: CA413657845
Gene: SLC16A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74525759G>T , CM000685.2:g.74525759G>T GRCh38
NC_000023.10:g.73745594G>T , CM000685.1:g.73745594G>T GRCh37
NC_000023.9:g.73662319G>T NCBI36
NG_011641.1:g.109510G>T
NG_011641.2:g.109510G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000587091.6:c.1036G>T MANE Select ENSP00000465734.1:p.Val346Leu
ENST00000636771.1:c.945G>T
ENST00000587091.5:c.1036G>T ENSP00000465734.1:p.Val346Leu
ENST00000590447.1:c.476G>T
NM_006517.4:c.1036G>T NP_006508.2:p.Val346Leu
XM_005262294.1:c.1036G>T XP_005262351.1:p.Val346Leu
XM_011531015.1:c.*40G>T XP_011529317.1:n.*40G>T
NM_006517.5:c.1036G>T MANE Select NP_006508.2:p.Val346Leu