Canonical Allele Identifier: CA1977295712

Gene: TMEM216

Linked Data

• dbSNP Id: rs1858697149

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392613_61392634del , CM000673.2:g.61392613_61392634del	GRCh38
NC_000011.9:g.61160085_61160106del , CM000673.1:g.61160085_61160106del	GRCh37
NC_000011.8:g.60916661_60916682del	NCBI36
NG_032976.1:g.5254_5275del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.-19_3del
ENST00000544795.6:n.27_48del
ENST00000690736.1:c.-19_3del
ENST00000515837.7:c.-19_3del
ENST00000334888.9:c.-19_3del
ENST00000398979.7:c.-216_-195del	ENSP00000381950.3:n.-216_-195del
ENST00000515837.6:c.-19_3del
NM_001173990.2:c.-19_3del
NM_001173991.2:c.-19_3del
NM_016499.5:c.-216_-195del	NP_057583.2:n.-216_-195del
XM_005274039.3:c.-350_-329del	XP_005274096.1:n.-350_-329del
NM_001330285.1:c.-216_-195del	NP_001317214.1:n.-216_-195del
XM_005274039.4:c.-350_-329del	XP_005274096.1:n.-350_-329del
NM_001173990.3:c.-19_3del
NM_001173991.3:c.-19_3del
NM_001330285.2:c.-216_-195del	NP_001317214.1:n.-216_-195del
NM_016499.6:c.-216_-195del	NP_057583.2:n.-216_-195del