Canonical Allele Identifier: CA1977295668
Gene: TMEM216 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392593G= , CM000673.2:g.61392593G= GRCh38
NC_000011.9:g.61160065G= , CM000673.1:g.61160065G= GRCh37
NC_000011.8:g.60916641G= NCBI36
NG_032976.1:g.5234G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000334888.10:c.-39G= ENSP00000334844.5:n.-39G=
ENST00000544795.6:n.7G=
ENST00000690736.1:c.-39G= ENSP00000508542.1:n.-39G=
ENST00000515837.7:c.-39G= MANE Select ENSP00000440638.1:n.-39G=
ENST00000334888.9:c.-39G= ENSP00000334844.5:n.-39G=
ENST00000398979.7:c.-236G= ENSP00000381950.3:n.-236G=
ENST00000515837.6:c.-39G= ENSP00000440638.1:n.-39G=
NM_001173990.2:c.-39G= NP_001167461.1:n.-39G=
NM_001173991.2:c.-39G= NP_001167462.1:n.-39G=
NM_016499.5:c.-236G= NP_057583.2:n.-236G=
XM_005274039.3:c.-370G= XP_005274096.1:n.-370G=
NM_001330285.1:c.-236G= NP_001317214.1:n.-236G=
XM_005274039.4:c.-370G= XP_005274096.1:n.-370G=
NM_001173990.3:c.-39G= MANE Select NP_001167461.1:n.-39G=
NM_001173991.3:c.-39G= NP_001167462.1:n.-39G=
NM_001330285.2:c.-236G= NP_001317214.1:n.-236G=
NM_016499.6:c.-236G= NP_057583.2:n.-236G=