Canonical Allele Identifier: CA2613835841
Gene: TMEM216 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392318_61392330del , CM000673.2:g.61392318_61392330del GRCh38
NC_000011.9:g.61159790_61159802del , CM000673.1:g.61159790_61159802del GRCh37
NC_000011.8:g.60916366_60916378del NCBI36
NG_032976.1:g.4959_4971del

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-314_-302del ENSP00000440638.1:n.-314_-302del
XM_005274039.3:c.-645_-633del XP_005274096.1:n.-645_-633del
XM_005274039.4:c.-645_-633del XP_005274096.1:n.-645_-633del