Canonical Allele Identifier: CA2613836379

Gene: TMEM216

Linked Data

• gnomAD v4: 11-61392620-C-CGGGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392620_61392621insGGGGGGG , CM000673.2:g.61392620_61392621insGGGGGGG	GRCh38
NC_000011.9:g.61160092_61160093insGGGGGGG , CM000673.1:g.61160092_61160093insGGGGGGG	GRCh37
NC_000011.8:g.60916668_60916669insGGGGGGG	NCBI36
NG_032976.1:g.5261_5262insGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.-12_-11insGGGGGGG	ENSP00000334844.5:n.-12_-11insGGGGGGG
ENST00000544795.6:n.34_35insGGGGGGG
ENST00000688959.1:c.-285_-284insGGGGGGG	ENSP00000509213.1:n.-285_-284insGGGGGGG
ENST00000690736.1:c.-12_-11insGGGGGGG	ENSP00000508542.1:n.-12_-11insGGGGGGG
ENST00000515837.7:c.-12_-11insGGGGGGG MANE Select	ENSP00000440638.1:n.-12_-11insGGGGGGG
ENST00000334888.9:c.-12_-11insGGGGGGG	ENSP00000334844.5:n.-12_-11insGGGGGGG
ENST00000398979.7:c.-209_-208insGGGGGGG	ENSP00000381950.3:n.-209_-208insGGGGGGG
ENST00000515837.6:c.-12_-11insGGGGGGG	ENSP00000440638.1:n.-12_-11insGGGGGGG
NM_001173990.2:c.-12_-11insGGGGGGG	NP_001167461.1:n.-12_-11insGGGGGGG
NM_001173991.2:c.-12_-11insGGGGGGG	NP_001167462.1:n.-12_-11insGGGGGGG
NM_016499.5:c.-209_-208insGGGGGGG	NP_057583.2:n.-209_-208insGGGGGGG
XM_005274039.3:c.-343_-342insGGGGGGG	XP_005274096.1:n.-343_-342insGGGGGGG
NM_001330285.1:c.-209_-208insGGGGGGG	NP_001317214.1:n.-209_-208insGGGGGGG
XM_005274039.4:c.-343_-342insGGGGGGG	XP_005274096.1:n.-343_-342insGGGGGGG
NM_001173990.3:c.-12_-11insGGGGGGG MANE Select	NP_001167461.1:n.-12_-11insGGGGGGG
NM_001173991.3:c.-12_-11insGGGGGGG	NP_001167462.1:n.-12_-11insGGGGGGG
NM_001330285.2:c.-209_-208insGGGGGGG	NP_001317214.1:n.-209_-208insGGGGGGG
NM_016499.6:c.-209_-208insGGGGGGG	NP_057583.2:n.-209_-208insGGGGGGG