Canonical Allele Identifier: CA2613835821
Gene: TMEM216 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392300del , CM000673.2:g.61392300del GRCh38
NC_000011.9:g.61159772del , CM000673.1:g.61159772del GRCh37
NC_000011.8:g.60916348del NCBI36
NG_032976.1:g.4941del

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-332del ENSP00000440638.1:n.-332del
XM_005274039.3:c.-663del XP_005274096.1:n.-663del
XM_005274039.4:c.-663del XP_005274096.1:n.-663del