Canonical Allele Identifier: CA2613836253
Gene: TMEM216 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392512_61392513insGGCA , CM000673.2:g.61392512_61392513insGGCA GRCh38
NC_000011.9:g.61159984_61159985insGGCA , CM000673.1:g.61159984_61159985insGGCA GRCh37
NC_000011.8:g.60916560_60916561insGGCA NCBI36
NG_032976.1:g.5153_5154insGGCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000334888.9:c.-120_-119insGGCA ENSP00000334844.5:n.-120_-119insGGCA
ENST00000398979.7:c.-317_-316insGGCA ENSP00000381950.3:n.-317_-316insGGCA
ENST00000515837.6:c.-120_-119insGGCA ENSP00000440638.1:n.-120_-119insGGCA
NM_001173990.2:c.-120_-119insGGCA NP_001167461.1:n.-120_-119insGGCA
NM_001173991.2:c.-120_-119insGGCA NP_001167462.1:n.-120_-119insGGCA
NM_016499.5:c.-317_-316insGGCA NP_057583.2:n.-317_-316insGGCA
XM_005274039.3:c.-451_-450insGGCA XP_005274096.1:n.-451_-450insGGCA
NM_001330285.1:c.-317_-316insGGCA NP_001317214.1:n.-317_-316insGGCA
XM_005274039.4:c.-451_-450insGGCA XP_005274096.1:n.-451_-450insGGCA