Canonical Allele Identifier: CA2613835796
Gene: TMEM216 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392274_61392275del , CM000673.2:g.61392274_61392275del GRCh38
NC_000011.9:g.61159746_61159747del , CM000673.1:g.61159746_61159747del GRCh37
NC_000011.8:g.60916322_60916323del NCBI36
NG_032976.1:g.4915_4916del

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-358_-357del ENSP00000440638.1:n.-358_-357del
XM_005274039.3:c.-689_-688del XP_005274096.1:n.-689_-688del
XM_005274039.4:c.-689_-688del XP_005274096.1:n.-689_-688del