Canonical Allele Identifier: CA2792320105

Gene: TMEM216

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392880_61392881insGCCTAGAAGTGGCCCAGC , CM000673.2:g.61392880_61392881insGCCTAGAAGTGGCCCAGC	GRCh38
NC_000011.9:g.61160352_61160353insGCCTAGAAGTGGCCCAGC , CM000673.1:g.61160352_61160353insGCCTAGAAGTGGCCCAGC	GRCh37
NC_000011.8:g.60916928_60916929insGCCTAGAAGTGGCCCAGC	NCBI36
NG_032976.1:g.5521_5522insGCCTAGAAGTGGCCCAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.34+215_34+216insGCCTAGAAGTGGCCCAGC	ENSP00000334844.5:n.34+215_34+216insGCCTAGAAGTGGCCCAGC
ENST00000544795.6:n.294_295insGCCTAGAAGTGGCCCAGC
ENST00000684926.1:n.50+201_50+202insGCCTAGAAGTGGCCCAGC
ENST00000688959.1:c.-226+201_-226+202insGCCTAGAAGTGGCCCAGC	ENSP00000509213.1:n.-226+201_-226+202insGCCTAGAAGTGGCCCAGC
ENST00000690736.1:c.34+215_34+216insGCCTAGAAGTGGCCCAGC	ENSP00000508542.1:n.34+215_34+216insGCCTAGAAGTGGCCCAGC
ENST00000515837.7:c.34+215_34+216insGCCTAGAAGTGGCCCAGC MANE Select	ENSP00000440638.1:n.34+215_34+216insGCCTAGAAGTGGCCCAGC
ENST00000334888.9:c.34+215_34+216insGCCTAGAAGTGGCCCAGC	ENSP00000334844.5:n.34+215_34+216insGCCTAGAAGTGGCCCAGC
ENST00000398979.7:c.-150+201_-150+202insGCCTAGAAGTGGCCCAGC	ENSP00000381950.3:n.-150+201_-150+202insGCCTAGAAGTGGCCCAGC
ENST00000515837.6:c.34+215_34+216insGCCTAGAAGTGGCCCAGC	ENSP00000440638.1:n.34+215_34+216insGCCTAGAAGTGGCCCAGC
ENST00000541473.1:n.48+201_48+202insGCCTAGAAGTGGCCCAGC
ENST00000544795.5:n.50+201_50+202insGCCTAGAAGTGGCCCAGC
NM_001173990.2:c.34+215_34+216insGCCTAGAAGTGGCCCAGC	NP_001167461.1:n.34+215_34+216insGCCTAGAAGTGGCCCAGC
NM_001173991.2:c.34+215_34+216insGCCTAGAAGTGGCCCAGC	NP_001167462.1:n.34+215_34+216insGCCTAGAAGTGGCCCAGC
NM_016499.5:c.-150+201_-150+202insGCCTAGAAGTGGCCCAGC	NP_057583.2:n.-150+201_-150+202insGCCTAGAAGTGGCCCAGC
XM_005274039.3:c.-167_-166insGCCTAGAAGTGGCCCAGC	XP_005274096.1:n.-167_-166insGCCTAGAAGTGGCCCAGC
NM_001330285.1:c.-150+201_-150+202insGCCTAGAAGTGGCCCAGC	NP_001317214.1:n.-150+201_-150+202insGCCTAGAAGTGGCCCAGC
XM_005274039.4:c.-167_-166insGCCTAGAAGTGGCCCAGC	XP_005274096.1:n.-167_-166insGCCTAGAAGTGGCCCAGC
NM_001173990.3:c.34+215_34+216insGCCTAGAAGTGGCCCAGC MANE Select	NP_001167461.1:n.34+215_34+216insGCCTAGAAGTGGCCCAGC
NM_001173991.3:c.34+215_34+216insGCCTAGAAGTGGCCCAGC	NP_001167462.1:n.34+215_34+216insGCCTAGAAGTGGCCCAGC
NM_001330285.2:c.-150+201_-150+202insGCCTAGAAGTGGCCCAGC	NP_001317214.1:n.-150+201_-150+202insGCCTAGAAGTGGCCCAGC
NM_016499.6:c.-150+201_-150+202insGCCTAGAAGTGGCCCAGC	NP_057583.2:n.-150+201_-150+202insGCCTAGAAGTGGCCCAGC