Canonical Allele Identifier: CA1977295462
Gene: TMEM216 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392402_61392403delinsTC , CM000673.2:g.61392402_61392403delinsTC GRCh38
NC_000011.9:g.61159874_61159875delinsTC , CM000673.1:g.61159874_61159875delinsTC GRCh37
NC_000011.8:g.60916450_60916451delinsTC NCBI36
NG_032976.1:g.5043_5044delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000334888.9:c.-230_-229delinsTC ENSP00000334844.5:n.-230_-229delinsTC
ENST00000398979.7:c.-427_-426delinsTC ENSP00000381950.3:n.-427_-426delinsTC
ENST00000515837.6:c.-230_-229delinsTC ENSP00000440638.1:n.-230_-229delinsTC
NM_001173990.2:c.-230_-229delinsTC NP_001167461.1:n.-230_-229delinsTC
NM_001173991.2:c.-230_-229delinsTC NP_001167462.1:n.-230_-229delinsTC
NM_016499.5:c.-427_-426delinsTC NP_057583.2:n.-427_-426delinsTC
XM_005274039.3:c.-561_-560delinsTC XP_005274096.1:n.-561_-560delinsTC
NM_001330285.1:c.-427_-426delinsTC NP_001317214.1:n.-427_-426delinsTC
XM_005274039.4:c.-561_-560delinsTC XP_005274096.1:n.-561_-560delinsTC