Canonical Allele Identifier: CA657732820
Gene: SLC16A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74529167del , CM000685.2:g.74529167del GRCh38
NC_000023.10:g.73749002del , CM000685.1:g.73749002del GRCh37
NC_000023.9:g.73665727del NCBI36
NG_011641.1:g.112918del
NG_011641.2:g.112918del

Transcript Alleles

HGVS Amino-acid change
ENST00000587091.6:c.1171-46del MANE Select ENSP00000465734.1:n.1171-46del
ENST00000636771.1:c.1080-46del
ENST00000587091.5:c.1171-46del ENSP00000465734.1:n.1171-46del
ENST00000590447.1:c.611-2166del
NM_006517.4:c.1171-46del NP_006508.2:n.1171-46del
XM_005262294.1:c.1171-2166del XP_005262351.1:n.1171-2166del
NM_006517.5:c.1171-46del MANE Select NP_006508.2:n.1171-46del