Canonical Allele Identifier: CA1977295847
Gene: TMEM216 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392672T= , CM000673.2:g.61392672T= GRCh38
NC_000011.9:g.61160144T= , CM000673.1:g.61160144T= GRCh37
NC_000011.8:g.60916720T= NCBI36
NG_032976.1:g.5313T=

Transcript Alleles

HGVS Amino-acid change
ENST00000334888.10:c.34+7T= ENSP00000334844.5:n.34+7T=
ENST00000544795.6:n.86T=
ENST00000684926.1:n.43T=
ENST00000688959.1:c.-233T= ENSP00000509213.1:n.-233T=
ENST00000690736.1:c.34+7T= ENSP00000508542.1:n.34+7T=
ENST00000515837.7:c.34+7T= MANE Select ENSP00000440638.1:n.34+7T=
ENST00000334888.9:c.34+7T= ENSP00000334844.5:n.34+7T=
ENST00000398979.7:c.-157T= ENSP00000381950.3:n.-157T=
ENST00000515837.6:c.34+7T= ENSP00000440638.1:n.34+7T=
ENST00000541473.1:n.41T=
ENST00000544795.5:n.43T=
NM_001173990.2:c.34+7T= NP_001167461.1:n.34+7T=
NM_001173991.2:c.34+7T= NP_001167462.1:n.34+7T=
NM_016499.5:c.-157T= NP_057583.2:n.-157T=
XM_005274039.3:c.-291T= XP_005274096.1:n.-291T=
NM_001330285.1:c.-157T= NP_001317214.1:n.-157T=
XM_005274039.4:c.-291T= XP_005274096.1:n.-291T=
NM_001173990.3:c.34+7T= MANE Select NP_001167461.1:n.34+7T=
NM_001173991.3:c.34+7T= NP_001167462.1:n.34+7T=
NM_001330285.2:c.-157T= NP_001317214.1:n.-157T=
NM_016499.6:c.-157T= NP_057583.2:n.-157T=