Canonical Allele Identifier: CA413656438
Gene: SLC16A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74422045T>G , CM000685.2:g.74422045T>G GRCh38
NC_000023.10:g.73641880T>G , CM000685.1:g.73641880T>G GRCh37
NC_000023.9:g.73558605T>G NCBI36
NG_011641.1:g.5796T>G
NG_011641.2:g.5796T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000587091.6:c.408T>G MANE Select ENSP00000465734.1:p.Asn136Lys
ENST00000636771.1:c.154T>G
ENST00000587091.5:c.408T>G ENSP00000465734.1:p.Asn136Lys
NM_006517.4:c.408T>G NP_006508.2:p.Asn136Lys
XM_005262294.1:c.408T>G XP_005262351.1:p.Asn136Lys
XM_011531015.1:c.408T>G XP_011529317.1:p.Asn136Lys
NM_006517.5:c.408T>G MANE Select NP_006508.2:p.Asn136Lys