Canonical Allele Identifier: CA413655854
Gene: SLC16A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74421774T>C , CM000685.2:g.74421774T>C GRCh38
NC_000023.10:g.73641609T>C , CM000685.1:g.73641609T>C GRCh37
NC_000023.9:g.73558334T>C NCBI36
NG_011641.1:g.5525T>C
NG_011641.2:g.5525T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000587091.6:c.137T>C MANE Select ENSP00000465734.1:p.Val46Ala
ENST00000587091.5:c.137T>C ENSP00000465734.1:p.Val46Ala
NM_006517.4:c.137T>C NP_006508.2:p.Val46Ala
XM_005262294.1:c.137T>C XP_005262351.1:p.Val46Ala
XM_011531015.1:c.137T>C XP_011529317.1:p.Val46Ala
NM_006517.5:c.137T>C MANE Select NP_006508.2:p.Val46Ala