Canonical Allele Identifier: CA1977295878
Gene: TMEM216 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392691G= , CM000673.2:g.61392691G= GRCh38
NC_000011.9:g.61160163G= , CM000673.1:g.61160163G= GRCh37
NC_000011.8:g.60916739G= NCBI36
NG_032976.1:g.5332G=

Transcript Alleles

HGVS Amino-acid change
ENST00000334888.10:c.34+26G= ENSP00000334844.5:n.34+26G=
ENST00000544795.6:n.105G=
ENST00000684926.1:n.50+12G=
ENST00000688959.1:c.-226+12G= ENSP00000509213.1:n.-226+12G=
ENST00000690736.1:c.34+26G= ENSP00000508542.1:n.34+26G=
ENST00000515837.7:c.34+26G= MANE Select ENSP00000440638.1:n.34+26G=
ENST00000334888.9:c.34+26G= ENSP00000334844.5:n.34+26G=
ENST00000398979.7:c.-150+12G= ENSP00000381950.3:n.-150+12G=
ENST00000515837.6:c.34+26G= ENSP00000440638.1:n.34+26G=
ENST00000541473.1:n.48+12G=
ENST00000544795.5:n.50+12G=
NM_001173990.2:c.34+26G= NP_001167461.1:n.34+26G=
NM_001173991.2:c.34+26G= NP_001167462.1:n.34+26G=
NM_016499.5:c.-150+12G= NP_057583.2:n.-150+12G=
XM_005274039.3:c.-284+12G= XP_005274096.1:n.-284+12G=
NM_001330285.1:c.-150+12G= NP_001317214.1:n.-150+12G=
XM_005274039.4:c.-284+12G= XP_005274096.1:n.-284+12G=
NM_001173990.3:c.34+26G= MANE Select NP_001167461.1:n.34+26G=
NM_001173991.3:c.34+26G= NP_001167462.1:n.34+26G=
NM_001330285.2:c.-150+12G= NP_001317214.1:n.-150+12G=
NM_016499.6:c.-150+12G= NP_057583.2:n.-150+12G=