Canonical Allele Identifier: CA1977295833

Gene: TMEM216

Linked Data

• dbSNP Id: rs1858700431

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392662_61392676del , CM000673.2:g.61392662_61392676del	GRCh38
NC_000011.9:g.61160134_61160148del , CM000673.1:g.61160134_61160148del	GRCh37
NC_000011.8:g.60916710_60916724del	NCBI36
NG_032976.1:g.5303_5317del

Transcript Alleles

HGVS	Amino-acid change
ENST00000334888.10:c.31_34+11del
ENST00000544795.6:n.76_90del
ENST00000684926.1:n.33_47del
ENST00000688959.1:c.-243_-229del	ENSP00000509213.1:n.-243_-229del
ENST00000690736.1:c.31_34+11del
ENST00000515837.7:c.31_34+11del
ENST00000334888.9:c.31_34+11del
ENST00000398979.7:c.-167_-153del	ENSP00000381950.3:n.-167_-153del
ENST00000515837.6:c.31_34+11del
ENST00000541473.1:n.31_45del
ENST00000544795.5:n.33_47del
NM_001173990.2:c.31_34+11del
NM_001173991.2:c.31_34+11del
NM_016499.5:c.-167_-153del	NP_057583.2:n.-167_-153del
XM_005274039.3:c.-301_-287del	XP_005274096.1:n.-301_-287del
NM_001330285.1:c.-167_-153del	NP_001317214.1:n.-167_-153del
XM_005274039.4:c.-301_-287del	XP_005274096.1:n.-301_-287del
NM_001173990.3:c.31_34+11del
NM_001173991.3:c.31_34+11del
NM_001330285.2:c.-167_-153del	NP_001317214.1:n.-167_-153del
NM_016499.6:c.-167_-153del	NP_057583.2:n.-167_-153del