Canonical Allele Identifier: CA413658502
Gene: SLC16A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74529370A>G , CM000685.2:g.74529370A>G GRCh38
NC_000023.10:g.73749205A>G , CM000685.1:g.73749205A>G GRCh37
NC_000023.9:g.73665930A>G NCBI36
NG_011641.1:g.113121A>G
NG_011641.2:g.113121A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000587091.6:c.1328A>G MANE Select ENSP00000465734.1:p.Gln443Arg
ENST00000636771.1:c.1237A>G
ENST00000587091.5:c.1328A>G ENSP00000465734.1:p.Gln443Arg
ENST00000590447.1:c.611-1963A>G
NM_006517.4:c.1328A>G NP_006508.2:p.Gln443Arg
XM_005262294.1:c.1171-1963A>G XP_005262351.1:n.1171-1963A>G
NM_006517.5:c.1328A>G MANE Select NP_006508.2:p.Gln443Arg