Canonical Allele Identifier: CA222894219
Gene: TMEM216 HGNC NCBI

Linked Data

dbSNP Id: rs1004611770

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392497del , CM000673.2:g.61392497del GRCh38
NC_000011.9:g.61159969del , CM000673.1:g.61159969del GRCh37
NC_000011.8:g.60916545del NCBI36
NG_032976.1:g.5138del

Transcript Alleles

HGVS Amino-acid Change
ENST00000334888.9:c.-135del ENSP00000334844.5:n.-135del
ENST00000398979.7:c.-332del ENSP00000381950.3:n.-332del
ENST00000515837.6:c.-135del ENSP00000440638.1:n.-135del
NM_001173990.2:c.-135del NP_001167461.1:n.-135del
NM_001173991.2:c.-135del NP_001167462.1:n.-135del
NM_016499.5:c.-332del NP_057583.2:n.-332del
XM_005274039.3:c.-466del XP_005274096.1:n.-466del
NM_001330285.1:c.-332del NP_001317214.1:n.-332del
XM_005274039.4:c.-466del XP_005274096.1:n.-466del