Canonical Allele Identifier: CA599502981

Gene: TMEM216

Linked Data

• dbSNP Id: rs1565087897
• gnomAD v2: 11-61160082-CCGGGAGCCGCTGTGGCAGCGTATGCTGCCA-C
• gnomAD v4: 11-61392610-CCGGGAGCCGCTGTGGCAGCGTATGCTGCCA-C
• MyVariant Identifiers: chr11:g.61160083_61160112del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392615_61392644del , CM000673.2:g.61392615_61392644del	GRCh38
NC_000011.9:g.61160087_61160116del , CM000673.1:g.61160087_61160116del	GRCh37
NC_000011.8:g.60916663_60916692del	NCBI36
NG_032976.1:g.5256_5285del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.-17_13del
ENST00000544795.6:n.29_58del
ENST00000690736.1:c.-17_13del
ENST00000515837.7:c.-17_13del
ENST00000334888.9:c.-17_13del
ENST00000398979.7:c.-214_-185del	ENSP00000381950.3:n.-214_-185del
ENST00000515837.6:c.-17_13del
NM_001173990.2:c.-17_13del
NM_001173991.2:c.-17_13del
NM_016499.5:c.-214_-185del	NP_057583.2:n.-214_-185del
XM_005274039.3:c.-348_-319del	XP_005274096.1:n.-348_-319del
NM_001330285.1:c.-214_-185del	NP_001317214.1:n.-214_-185del
XM_005274039.4:c.-348_-319del	XP_005274096.1:n.-348_-319del
NM_001173990.3:c.-17_13del
NM_001173991.3:c.-17_13del
NM_001330285.2:c.-214_-185del	NP_001317214.1:n.-214_-185del
NM_016499.6:c.-214_-185del	NP_057583.2:n.-214_-185del