Canonical Allele Identifier: CA2613836367

Gene: TMEM216

Linked Data

• gnomAD v4: 11-61392620-CTGTGGCAGCGTAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392621_61392633del , CM000673.2:g.61392621_61392633del	GRCh38
NC_000011.9:g.61160093_61160105del , CM000673.1:g.61160093_61160105del	GRCh37
NC_000011.8:g.60916669_60916681del	NCBI36
NG_032976.1:g.5262_5274del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.-11_2del
ENST00000544795.6:n.35_47del
ENST00000688959.1:c.-284_-272del	ENSP00000509213.1:n.-284_-272del
ENST00000690736.1:c.-11_2del
ENST00000515837.7:c.-11_2del
ENST00000334888.9:c.-11_2del
ENST00000398979.7:c.-208_-196del	ENSP00000381950.3:n.-208_-196del
ENST00000515837.6:c.-11_2del
NM_001173990.2:c.-11_2del
NM_001173991.2:c.-11_2del
NM_016499.5:c.-208_-196del	NP_057583.2:n.-208_-196del
XM_005274039.3:c.-342_-330del	XP_005274096.1:n.-342_-330del
NM_001330285.1:c.-208_-196del	NP_001317214.1:n.-208_-196del
XM_005274039.4:c.-342_-330del	XP_005274096.1:n.-342_-330del
NM_001173990.3:c.-11_2del
NM_001173991.3:c.-11_2del
NM_001330285.2:c.-208_-196del	NP_001317214.1:n.-208_-196del
NM_016499.6:c.-208_-196del	NP_057583.2:n.-208_-196del