Canonical Allele Identifier: CA1362234570
Gene: TMIE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46709188C= , CM000665.2:g.46709188C= GRCh38
NC_000003.11:g.46750678C= , CM000665.1:g.46750678C= GRCh37
NC_000003.10:g.46725682C= NCBI36
NG_011628.1:g.12856C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000643606.3:c.274C= MANE Select ENSP00000494576.2:p.Arg92=
ENST00000644830.1:c.115C= ENSP00000495111.1:p.Arg39=
ENST00000651652.1:c.172C= ENSP00000498953.1:p.Arg58=
ENST00000326431.3:c.274C= ENSP00000324775.3:p.Arg92=
NM_147196.2:c.274C= NP_671729.2:p.Arg92=
XM_006713097.2:c.115C= XP_006713160.1:p.Arg39=
XM_011533574.1:c.115C= XP_011531876.1:p.Arg39=
XM_006713097.4:c.115C= XP_006713160.1:p.Arg39=
XM_024453446.1:c.115C= XP_024309214.1:p.Arg39=
NM_001370524.1:c.115C= NP_001357453.1:p.Arg39=
NM_001370525.1:c.115C= NP_001357454.1:p.Arg39=
NM_147196.3:c.274C= MANE Select NP_671729.2:p.Arg92=