Canonical Allele Identifier: CA2665467476
Gene: TMIE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46709035del , CM000665.2:g.46709035del GRCh38
NC_000003.11:g.46750525del , CM000665.1:g.46750525del GRCh37
NC_000003.10:g.46725529del NCBI36
NG_011628.1:g.12703del

Transcript Alleles

HGVS Amino-acid Change
ENST00000643606.3:c.212-91del MANE Select ENSP00000494576.2:n.212-91del
ENST00000644830.1:c.53-91del ENSP00000495111.1:n.53-91del
ENST00000651652.1:c.110-91del ENSP00000498953.1:n.110-91del
ENST00000326431.3:c.212-91del ENSP00000324775.3:n.212-91del
NM_147196.2:c.212-91del NP_671729.2:n.212-91del
XM_006713097.2:c.53-91del XP_006713160.1:n.53-91del
XM_011533574.1:c.53-91del XP_011531876.1:n.53-91del
XM_006713097.4:c.53-91del XP_006713160.1:n.53-91del
XM_024453446.1:c.53-91del XP_024309214.1:n.53-91del
NM_001370524.1:c.53-91del NP_001357453.1:n.53-91del
NM_001370525.1:c.53-91del NP_001357454.1:n.53-91del
NM_147196.3:c.212-91del MANE Select NP_671729.2:n.212-91del