Canonical Allele Identifier: CA2613835799
Gene: TMEM216 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392276del , CM000673.2:g.61392276del GRCh38
NC_000011.9:g.61159748del , CM000673.1:g.61159748del GRCh37
NC_000011.8:g.60916324del NCBI36
NG_032976.1:g.4917del

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-356del ENSP00000440638.1:n.-356del
XM_005274039.3:c.-687del XP_005274096.1:n.-687del
XM_005274039.4:c.-687del XP_005274096.1:n.-687del