Canonical Allele Identifier: CA1977295508

Gene: TMEM216

Linked Data

• dbSNP Id: rs1858692069

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392469dup , CM000673.2:g.61392469dup	GRCh38
NC_000011.9:g.61159941dup , CM000673.1:g.61159941dup	GRCh37
NC_000011.8:g.60916517dup	NCBI36
NG_032976.1:g.5110dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.9:c.-163dup	ENSP00000334844.5:n.-163dup
ENST00000398979.7:c.-360dup	ENSP00000381950.3:n.-360dup
ENST00000515837.6:c.-163dup	ENSP00000440638.1:n.-163dup
NM_001173990.2:c.-163dup	NP_001167461.1:n.-163dup
NM_001173991.2:c.-163dup	NP_001167462.1:n.-163dup
NM_016499.5:c.-360dup	NP_057583.2:n.-360dup
XM_005274039.3:c.-494dup	XP_005274096.1:n.-494dup
NM_001330285.1:c.-360dup	NP_001317214.1:n.-360dup
XM_005274039.4:c.-494dup	XP_005274096.1:n.-494dup