Canonical Allele Identifier: CA413658051
Gene: SLC16A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74525852A>T , CM000685.2:g.74525852A>T GRCh38
NC_000023.10:g.73745687A>T , CM000685.1:g.73745687A>T GRCh37
NC_000023.9:g.73662412A>T NCBI36
NG_011641.1:g.109603A>T
NG_011641.2:g.109603A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000587091.6:c.1129A>T MANE Select ENSP00000465734.1:p.Ile377Phe
ENST00000636771.1:c.1038A>T
ENST00000587091.5:c.1129A>T ENSP00000465734.1:p.Ile377Phe
ENST00000590447.1:c.569A>T
NM_006517.4:c.1129A>T NP_006508.2:p.Ile377Phe
XM_005262294.1:c.1129A>T XP_005262351.1:p.Ile377Phe
NM_006517.5:c.1129A>T MANE Select NP_006508.2:p.Ile377Phe