Canonical Allele Identifier: CA2613839035

Gene: TMEM216

Linked Data

• gnomAD v4: 11-61397658-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61397663del , CM000673.2:g.61397663del	GRCh38
NC_000011.9:g.61165135del , CM000673.1:g.61165135del	GRCh37
NC_000011.8:g.60921711del	NCBI36
NG_032976.1:g.10304del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.230-111del	ENSP00000334844.5:n.230-111del
ENST00000544795.6:n.507-65del
ENST00000684926.1:n.246-65del
ENST00000688959.1:c.-21-119del	ENSP00000509213.1:n.-21-119del
ENST00000690736.1:c.230-65del	ENSP00000508542.1:n.230-65del
ENST00000515837.7:c.230-111del MANE Select	ENSP00000440638.1:n.230-111del
ENST00000334888.9:c.230-111del	ENSP00000334844.5:n.230-111del
ENST00000398979.7:c.47-111del	ENSP00000381950.3:n.47-111del
ENST00000515837.6:c.230-111del	ENSP00000440638.1:n.230-111del
ENST00000544795.5:n.246-65del
NM_001173990.2:c.230-111del	NP_001167461.1:n.230-111del
NM_001173991.2:c.230-111del	NP_001167462.1:n.230-111del
NM_016499.5:c.47-111del	NP_057583.2:n.47-111del
XM_005274039.3:c.47-111del	XP_005274096.1:n.47-111del
NM_001330285.1:c.47-111del	NP_001317214.1:n.47-111del
XM_005274039.4:c.47-111del	XP_005274096.1:n.47-111del
NM_001173990.3:c.230-111del MANE Select	NP_001167461.1:n.230-111del
NM_001173991.3:c.230-111del	NP_001167462.1:n.230-111del
NM_001330285.2:c.47-111del	NP_001317214.1:n.47-111del
NM_016499.6:c.47-111del	NP_057583.2:n.47-111del