Canonical Allele Identifier: CA2613835860
Gene: TMEM216 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392339del , CM000673.2:g.61392339del GRCh38
NC_000011.9:g.61159811del , CM000673.1:g.61159811del GRCh37
NC_000011.8:g.60916387del NCBI36
NG_032976.1:g.4980del

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-293del ENSP00000440638.1:n.-293del
XM_005274039.3:c.-624del XP_005274096.1:n.-624del
XM_005274039.4:c.-624del XP_005274096.1:n.-624del