Canonical Allele Identifier: CA599503260
Gene: TMEM216 HGNC NCBI

Linked Data

dbSNP Id: rs1320523370

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61393505_61393517del , CM000673.2:g.61393505_61393517del GRCh38
NC_000011.9:g.61160977_61160989del , CM000673.1:g.61160977_61160989del GRCh37
NC_000011.8:g.60917553_60917565del NCBI36
NG_032976.1:g.6146_6158del

Transcript Alleles

HGVS Amino-acid Change
ENST00000334888.10:c.136+173_136+185del ENSP00000334844.5:n.136+173_136+185del
ENST00000544795.6:n.413+173_413+185del
ENST00000684926.1:n.152+173_152+185del
ENST00000688959.1:c.-124+173_-124+185del ENSP00000509213.1:n.-124+173_-124+185del
ENST00000690736.1:c.136+173_136+185del ENSP00000508542.1:n.136+173_136+185del
ENST00000515837.7:c.136+173_136+185del MANE Select ENSP00000440638.1:n.136+173_136+185del
ENST00000334888.9:c.136+173_136+185del ENSP00000334844.5:n.136+173_136+185del
ENST00000398979.7:c.-48+173_-48+185del ENSP00000381950.3:n.-48+173_-48+185del
ENST00000515837.6:c.136+173_136+185del ENSP00000440638.1:n.136+173_136+185del
ENST00000541473.1:n.150+173_150+185del
ENST00000544795.5:n.152+173_152+185del
NM_001173990.2:c.136+173_136+185del NP_001167461.1:n.136+173_136+185del
NM_001173991.2:c.136+173_136+185del NP_001167462.1:n.136+173_136+185del
NM_016499.5:c.-48+173_-48+185del NP_057583.2:n.-48+173_-48+185del
XM_005274039.3:c.-48+173_-48+185del XP_005274096.1:n.-48+173_-48+185del
NM_001330285.1:c.-48+173_-48+185del NP_001317214.1:n.-48+173_-48+185del
XM_005274039.4:c.-48+173_-48+185del XP_005274096.1:n.-48+173_-48+185del
NM_001173990.3:c.136+173_136+185del MANE Select NP_001167461.1:n.136+173_136+185del
NM_001173991.3:c.136+173_136+185del NP_001167462.1:n.136+173_136+185del
NM_001330285.2:c.-48+173_-48+185del NP_001317214.1:n.-48+173_-48+185del
NM_016499.6:c.-48+173_-48+185del NP_057583.2:n.-48+173_-48+185del