Canonical Allele Identifier: CA2613837512
Gene: TMEM216 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61393816dup , CM000673.2:g.61393816dup GRCh38
NC_000011.9:g.61161288dup , CM000673.1:g.61161288dup GRCh37
NC_000011.8:g.60917864dup NCBI36
NG_032976.1:g.6457dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000334888.10:c.137-68dup ENSP00000334844.5:n.137-68dup
ENST00000544795.6:n.414-68dup
ENST00000684926.1:n.153-68dup
ENST00000688959.1:c.-123-68dup ENSP00000509213.1:n.-123-68dup
ENST00000690736.1:c.137-68dup ENSP00000508542.1:n.137-68dup
ENST00000515837.7:c.137-68dup MANE Select ENSP00000440638.1:n.137-68dup
ENST00000334888.9:c.137-68dup ENSP00000334844.5:n.137-68dup
ENST00000398979.7:c.-47-68dup ENSP00000381950.3:n.-47-68dup
ENST00000515837.6:c.137-68dup ENSP00000440638.1:n.137-68dup
ENST00000541473.1:n.151-68dup
ENST00000544795.5:n.153-68dup
NM_001173990.2:c.137-68dup NP_001167461.1:n.137-68dup
NM_001173991.2:c.137-68dup NP_001167462.1:n.137-68dup
NM_016499.5:c.-47-68dup NP_057583.2:n.-47-68dup
XM_005274039.3:c.-47-68dup XP_005274096.1:n.-47-68dup
NM_001330285.1:c.-47-68dup NP_001317214.1:n.-47-68dup
XM_005274039.4:c.-47-68dup XP_005274096.1:n.-47-68dup
NM_001173990.3:c.137-68dup MANE Select NP_001167461.1:n.137-68dup
NM_001173991.3:c.137-68dup NP_001167462.1:n.137-68dup
NM_001330285.2:c.-47-68dup NP_001317214.1:n.-47-68dup
NM_016499.6:c.-47-68dup NP_057583.2:n.-47-68dup