Canonical Allele Identifier: CA2694115311
Gene: SLC16A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74529166del , CM000685.2:g.74529166del GRCh38
NC_000023.10:g.73749001del , CM000685.1:g.73749001del GRCh37
NC_000023.9:g.73665726del NCBI36
NG_011641.1:g.112917del
NG_011641.2:g.112917del

Transcript Alleles

HGVS Amino-acid Change
ENST00000587091.6:c.1171-47del MANE Select ENSP00000465734.1:n.1171-47del
ENST00000636771.1:c.1080-47del
ENST00000587091.5:c.1171-47del ENSP00000465734.1:n.1171-47del
ENST00000590447.1:c.611-2167del
NM_006517.4:c.1171-47del NP_006508.2:n.1171-47del
XM_005262294.1:c.1171-2167del XP_005262351.1:n.1171-2167del
NM_006517.5:c.1171-47del MANE Select NP_006508.2:n.1171-47del