Canonical Allele Identifier: CA1977296217

Gene: TMEM216

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61393057_61393058delinsCT , CM000673.2:g.61393057_61393058delinsCT	GRCh38
NC_000011.9:g.61160529_61160530delinsCT , CM000673.1:g.61160529_61160530delinsCT	GRCh37
NC_000011.8:g.60917105_60917106delinsCT	NCBI36
NG_032976.1:g.5698_5699delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000334888.10:c.35-174_35-173delinsCT	ENSP00000334844.5:n.35-174_35-173delinsCT
ENST00000544795.6:n.311+160_311+161delinsCT
ENST00000684926.1:n.51-174_51-173delinsCT
ENST00000688959.1:c.-225-174_-225-173delinsCT	ENSP00000509213.1:n.-225-174_-225-173delinsCT
ENST00000690736.1:c.35-174_35-173delinsCT	ENSP00000508542.1:n.35-174_35-173delinsCT
ENST00000515837.7:c.35-174_35-173delinsCT MANE Select	ENSP00000440638.1:n.35-174_35-173delinsCT
ENST00000334888.9:c.35-174_35-173delinsCT	ENSP00000334844.5:n.35-174_35-173delinsCT
ENST00000398979.7:c.-149-174_-149-173delinsCT	ENSP00000381950.3:n.-149-174_-149-173delinsCT
ENST00000515837.6:c.35-174_35-173delinsCT	ENSP00000440638.1:n.35-174_35-173delinsCT
ENST00000541473.1:n.49-174_49-173delinsCT
ENST00000544795.5:n.51-174_51-173delinsCT
NM_001173990.2:c.35-174_35-173delinsCT	NP_001167461.1:n.35-174_35-173delinsCT
NM_001173991.2:c.35-174_35-173delinsCT	NP_001167462.1:n.35-174_35-173delinsCT
NM_016499.5:c.-149-174_-149-173delinsCT	NP_057583.2:n.-149-174_-149-173delinsCT
XM_005274039.3:c.-150+160_-150+161delinsCT	XP_005274096.1:n.-150+160_-150+161delinsCT
NM_001330285.1:c.-149-174_-149-173delinsCT	NP_001317214.1:n.-149-174_-149-173delinsCT
XM_005274039.4:c.-150+160_-150+161delinsCT	XP_005274096.1:n.-150+160_-150+161delinsCT
NM_001173990.3:c.35-174_35-173delinsCT MANE Select	NP_001167461.1:n.35-174_35-173delinsCT
NM_001173991.3:c.35-174_35-173delinsCT	NP_001167462.1:n.35-174_35-173delinsCT
NM_001330285.2:c.-149-174_-149-173delinsCT	NP_001317214.1:n.-149-174_-149-173delinsCT
NM_016499.6:c.-149-174_-149-173delinsCT	NP_057583.2:n.-149-174_-149-173delinsCT