Canonical Allele Identifier: CA2792320038
Gene: TMEM216 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392525_61392526insTTCTCGTTCCGGTCATCCTCAACGCC , CM000673.2:g.61392525_61392526insTTCTCGTTCCGGTCATCCTCAACGCC GRCh38
NC_000011.9:g.61159997_61159998insTTCTCGTTCCGGTCATCCTCAACGCC , CM000673.1:g.61159997_61159998insTTCTCGTTCCGGTCATCCTCAACGCC GRCh37
NC_000011.8:g.60916573_60916574insTTCTCGTTCCGGTCATCCTCAACGCC NCBI36
NG_032976.1:g.5166_5167insTTCTCGTTCCGGTCATCCTCAACGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000334888.9:c.-107_-106insTTCTCGTTCCGGTCATCCTCAACGCC ENSP00000334844.5:n.-107_-106insTTCTCGTTCCGGTCATCCTCAACGCC
ENST00000398979.7:c.-304_-303insTTCTCGTTCCGGTCATCCTCAACGCC ENSP00000381950.3:n.-304_-303insTTCTCGTTCCGGTCATCCTCAACGCC
ENST00000515837.6:c.-107_-106insTTCTCGTTCCGGTCATCCTCAACGCC ENSP00000440638.1:n.-107_-106insTTCTCGTTCCGGTCATCCTCAACGCC
NM_001173990.2:c.-107_-106insTTCTCGTTCCGGTCATCCTCAACGCC NP_001167461.1:n.-107_-106insTTCTCGTTCCGGTCATCCTCAACGCC
NM_001173991.2:c.-107_-106insTTCTCGTTCCGGTCATCCTCAACGCC NP_001167462.1:n.-107_-106insTTCTCGTTCCGGTCATCCTCAACGCC
NM_016499.5:c.-304_-303insTTCTCGTTCCGGTCATCCTCAACGCC NP_057583.2:n.-304_-303insTTCTCGTTCCGGTCATCCTCAACGCC
XM_005274039.3:c.-438_-437insTTCTCGTTCCGGTCATCCTCAACGCC XP_005274096.1:n.-438_-437insTTCTCGTTCCGGTCATCCTCAACGCC
NM_001330285.1:c.-304_-303insTTCTCGTTCCGGTCATCCTCAACGCC NP_001317214.1:n.-304_-303insTTCTCGTTCCGGTCATCCTCAACGCC
XM_005274039.4:c.-438_-437insTTCTCGTTCCGGTCATCCTCAACGCC XP_005274096.1:n.-438_-437insTTCTCGTTCCGGTCATCCTCAACGCC