Canonical Allele Identifier: CA1362233207
Gene: TMIE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46706016_46706017delinsCA , CM000665.2:g.46706016_46706017delinsCA GRCh38
NC_000003.11:g.46747506_46747507delinsCA , CM000665.1:g.46747506_46747507delinsCA GRCh37
NC_000003.10:g.46722510_46722511delinsCA NCBI36
NG_011628.1:g.9684_9685delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000643606.3:c.211+109_211+110delinsCA MANE Select ENSP00000494576.2:n.211+109_211+110delinsCA
ENST00000644830.1:c.52+109_52+110delinsCA ENSP00000495111.1:n.52+109_52+110delinsCA
ENST00000651652.1:c.109+109_109+110delinsCA ENSP00000498953.1:n.109+109_109+110delinsCA
ENST00000326431.3:c.211+109_211+110delinsCA ENSP00000324775.3:n.211+109_211+110delinsCA
NM_147196.2:c.211+109_211+110delinsCA NP_671729.2:n.211+109_211+110delinsCA
XM_006713097.2:c.52+109_52+110delinsCA XP_006713160.1:n.52+109_52+110delinsCA
XM_011533574.1:c.52+109_52+110delinsCA XP_011531876.1:n.52+109_52+110delinsCA
XM_006713097.4:c.52+109_52+110delinsCA XP_006713160.1:n.52+109_52+110delinsCA
XM_024453446.1:c.52+109_52+110delinsCA XP_024309214.1:n.52+109_52+110delinsCA
NM_001370524.1:c.52+109_52+110delinsCA NP_001357453.1:n.52+109_52+110delinsCA
NM_001370525.1:c.52+109_52+110delinsCA NP_001357454.1:n.52+109_52+110delinsCA
NM_147196.3:c.211+109_211+110delinsCA MANE Select NP_671729.2:n.211+109_211+110delinsCA