Canonical Allele Identifier: CA413656398
Gene: SLC16A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74422029A>T , CM000685.2:g.74422029A>T GRCh38
NC_000023.10:g.73641864A>T , CM000685.1:g.73641864A>T GRCh37
NC_000023.9:g.73558589A>T NCBI36
NG_011641.1:g.5780A>T
NG_011641.2:g.5780A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000587091.6:c.392A>T MANE Select ENSP00000465734.1:p.Glu131Val
ENST00000636771.1:c.138A>T
ENST00000587091.5:c.392A>T ENSP00000465734.1:p.Glu131Val
NM_006517.4:c.392A>T NP_006508.2:p.Glu131Val
XM_005262294.1:c.392A>T XP_005262351.1:p.Glu131Val
XM_011531015.1:c.392A>T XP_011529317.1:p.Glu131Val
NM_006517.5:c.392A>T MANE Select NP_006508.2:p.Glu131Val