Canonical Allele Identifier: CA1977295931

Gene: TMEM216

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392750_61392757delinsCCTCCATT , CM000673.2:g.61392750_61392757delinsCCTCCATT	GRCh38
NC_000011.9:g.61160222_61160229delinsCCTCCATT , CM000673.1:g.61160222_61160229delinsCCTCCATT	GRCh37
NC_000011.8:g.60916798_60916805delinsCCTCCATT	NCBI36
NG_032976.1:g.5391_5398delinsCCTCCATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.34+85_34+92delinsCCTCCATT	ENSP00000334844.5:n.34+85_34+92delinsCCTCCATT
ENST00000544795.6:n.164_171delinsCCTCCATT
ENST00000684926.1:n.50+71_50+78delinsCCTCCATT
ENST00000688959.1:c.-226+71_-226+78delinsCCTCCATT	ENSP00000509213.1:n.-226+71_-226+78delinsCCTCCATT
ENST00000690736.1:c.34+85_34+92delinsCCTCCATT	ENSP00000508542.1:n.34+85_34+92delinsCCTCCATT
ENST00000515837.7:c.34+85_34+92delinsCCTCCATT MANE Select	ENSP00000440638.1:n.34+85_34+92delinsCCTCCATT
ENST00000334888.9:c.34+85_34+92delinsCCTCCATT	ENSP00000334844.5:n.34+85_34+92delinsCCTCCATT
ENST00000398979.7:c.-150+71_-150+78delinsCCTCCATT	ENSP00000381950.3:n.-150+71_-150+78delinsCCTCCATT
ENST00000515837.6:c.34+85_34+92delinsCCTCCATT	ENSP00000440638.1:n.34+85_34+92delinsCCTCCATT
ENST00000541473.1:n.48+71_48+78delinsCCTCCATT
ENST00000544795.5:n.50+71_50+78delinsCCTCCATT
NM_001173990.2:c.34+85_34+92delinsCCTCCATT	NP_001167461.1:n.34+85_34+92delinsCCTCCATT
NM_001173991.2:c.34+85_34+92delinsCCTCCATT	NP_001167462.1:n.34+85_34+92delinsCCTCCATT
NM_016499.5:c.-150+71_-150+78delinsCCTCCATT	NP_057583.2:n.-150+71_-150+78delinsCCTCCATT
XM_005274039.3:c.-283-14_-283-7delinsCCTCCATT	XP_005274096.1:n.-283-14_-283-7delinsCCTCCATT
NM_001330285.1:c.-150+71_-150+78delinsCCTCCATT	NP_001317214.1:n.-150+71_-150+78delinsCCTCCATT
XM_005274039.4:c.-283-14_-283-7delinsCCTCCATT	XP_005274096.1:n.-283-14_-283-7delinsCCTCCATT
NM_001173990.3:c.34+85_34+92delinsCCTCCATT MANE Select	NP_001167461.1:n.34+85_34+92delinsCCTCCATT
NM_001173991.3:c.34+85_34+92delinsCCTCCATT	NP_001167462.1:n.34+85_34+92delinsCCTCCATT
NM_001330285.2:c.-150+71_-150+78delinsCCTCCATT	NP_001317214.1:n.-150+71_-150+78delinsCCTCCATT
NM_016499.6:c.-150+71_-150+78delinsCCTCCATT	NP_057583.2:n.-150+71_-150+78delinsCCTCCATT