Canonical Allele Identifier: CA413656200
Gene: SLC16A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74421940G>T , CM000685.2:g.74421940G>T GRCh38
NC_000023.10:g.73641775G>T , CM000685.1:g.73641775G>T GRCh37
NC_000023.9:g.73558500G>T NCBI36
NG_011641.1:g.5691G>T
NG_011641.2:g.5691G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000587091.6:c.303G>T MANE Select ENSP00000465734.1:p.Trp101Cys
ENST00000636771.1:c.49G>T
ENST00000587091.5:c.303G>T ENSP00000465734.1:p.Trp101Cys
NM_006517.4:c.303G>T NP_006508.2:p.Trp101Cys
XM_005262294.1:c.303G>T XP_005262351.1:p.Trp101Cys
XM_011531015.1:c.303G>T XP_011529317.1:p.Trp101Cys
NM_006517.5:c.303G>T MANE Select NP_006508.2:p.Trp101Cys