Canonical Allele Identifier: CA1977295859

Gene: TMEM216

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392679_61392683delinsGGTGT , CM000673.2:g.61392679_61392683delinsGGTGT	GRCh38
NC_000011.9:g.61160151_61160155delinsGGTGT , CM000673.1:g.61160151_61160155delinsGGTGT	GRCh37
NC_000011.8:g.60916727_60916731delinsGGTGT	NCBI36
NG_032976.1:g.5320_5324delinsGGTGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000334888.10:c.34+14_34+18delinsGGTGT	ENSP00000334844.5:n.34+14_34+18delinsGGTG...
ENST00000544795.6:n.93_97delinsGGTGT
ENST00000684926.1:n.50_50+4delinsGGTGT
ENST00000688959.1:c.-226_-226+4delinsGGTGT
ENST00000690736.1:c.34+14_34+18delinsGGTGT	ENSP00000508542.1:n.34+14_34+18delinsGGTG...
ENST00000515837.7:c.34+14_34+18delinsGGTGT MANE Select	ENSP00000440638.1:n.34+14_34+18delinsGGTG...
ENST00000334888.9:c.34+14_34+18delinsGGTGT	ENSP00000334844.5:n.34+14_34+18delinsGGTG...
ENST00000398979.7:c.-150_-150+4delinsGGTGT
ENST00000515837.6:c.34+14_34+18delinsGGTGT	ENSP00000440638.1:n.34+14_34+18delinsGGTG...
ENST00000541473.1:n.48_48+4delinsGGTGT
ENST00000544795.5:n.50_50+4delinsGGTGT
NM_001173990.2:c.34+14_34+18delinsGGTGT	NP_001167461.1:n.34+14_34+18delinsGGTGT
NM_001173991.2:c.34+14_34+18delinsGGTGT	NP_001167462.1:n.34+14_34+18delinsGGTGT
NM_016499.5:c.-150_-150+4delinsGGTGT
XM_005274039.3:c.-284_-284+4delinsGGTGT
NM_001330285.1:c.-150_-150+4delinsGGTGT
XM_005274039.4:c.-284_-284+4delinsGGTGT
NM_001173990.3:c.34+14_34+18delinsGGTGT MANE Select	NP_001167461.1:n.34+14_34+18delinsGGTGT
NM_001173991.3:c.34+14_34+18delinsGGTGT	NP_001167462.1:n.34+14_34+18delinsGGTGT
NM_001330285.2:c.-150_-150+4delinsGGTGT
NM_016499.6:c.-150_-150+4delinsGGTGT