Canonical Allele Identifier: CA352479033
Gene: TMIE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46705829A>T , CM000665.2:g.46705829A>T GRCh38
NC_000003.11:g.46747319A>T , CM000665.1:g.46747319A>T GRCh37
NC_000003.10:g.46722323A>T NCBI36
NG_011628.1:g.9497A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000643606.3:c.133A>T MANE Select ENSP00000494576.2:p.Thr45Ser
ENST00000644830.1:c.-27A>T ENSP00000495111.1:n.-27A>T
ENST00000651652.1:c.31A>T ENSP00000498953.1:p.Thr11Ser
ENST00000326431.3:c.133A>T ENSP00000324775.3:p.Thr45Ser
NM_147196.2:c.133A>T NP_671729.2:p.Thr45Ser
XM_006713097.2:c.-27A>T XP_006713160.1:n.-27A>T
XM_011533574.1:c.-27A>T XP_011531876.1:n.-27A>T
XM_006713097.4:c.-27A>T XP_006713160.1:n.-27A>T
XM_024453446.1:c.-27A>T XP_024309214.1:n.-27A>T
NM_001370524.1:c.-27A>T NP_001357453.1:n.-27A>T
NM_001370525.1:c.-27A>T NP_001357454.1:n.-27A>T
NM_147196.3:c.133A>T MANE Select NP_671729.2:p.Thr45Ser