Canonical Allele Identifier: CA2839730440

Gene: TMEM216

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61397743del , CM000673.2:g.61397743del	GRCh38
NC_000011.9:g.61165215del , CM000673.1:g.61165215del	GRCh37
NC_000011.8:g.60921791del	NCBI36
NG_032976.1:g.10384del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.230-31del	ENSP00000334844.5:n.230-31del
ENST00000544795.6:n.522del
ENST00000684926.1:n.261del
ENST00000688959.1:c.-21-39del	ENSP00000509213.1:n.-21-39del
ENST00000690736.1:c.245del	ENSP00000508542.1:p.Leu82TrpfsTer3
ENST00000515837.7:c.230-31del MANE Select	ENSP00000440638.1:n.230-31del
ENST00000334888.9:c.230-31del	ENSP00000334844.5:n.230-31del
ENST00000398979.7:c.47-31del	ENSP00000381950.3:n.47-31del
ENST00000515837.6:c.230-31del	ENSP00000440638.1:n.230-31del
ENST00000544795.5:n.261del
NM_001173990.2:c.230-31del	NP_001167461.1:n.230-31del
NM_001173991.2:c.230-31del	NP_001167462.1:n.230-31del
NM_016499.5:c.47-31del	NP_057583.2:n.47-31del
XM_005274039.3:c.47-31del	XP_005274096.1:n.47-31del
NM_001330285.1:c.47-31del	NP_001317214.1:n.47-31del
XM_005274039.4:c.47-31del	XP_005274096.1:n.47-31del
NM_001173990.3:c.230-31del MANE Select	NP_001167461.1:n.230-31del
NM_001173991.3:c.230-31del	NP_001167462.1:n.230-31del
NM_001330285.2:c.47-31del	NP_001317214.1:n.47-31del
NM_016499.6:c.47-31del	NP_057583.2:n.47-31del