Canonical Allele Identifier: CA352480652
Gene: TMIE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46709176G>T , CM000665.2:g.46709176G>T GRCh38
NC_000003.11:g.46750666G>T , CM000665.1:g.46750666G>T GRCh37
NC_000003.10:g.46725670G>T NCBI36
NG_011628.1:g.12844G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000643606.3:c.262G>T MANE Select ENSP00000494576.2:p.Glu88Ter
ENST00000644830.1:c.103G>T ENSP00000495111.1:p.Glu35Ter
ENST00000651652.1:c.160G>T ENSP00000498953.1:p.Glu54Ter
ENST00000326431.3:c.262G>T ENSP00000324775.3:p.Glu88Ter
NM_147196.2:c.262G>T NP_671729.2:p.Glu88Ter
XM_006713097.2:c.103G>T XP_006713160.1:p.Glu35Ter
XM_011533574.1:c.103G>T XP_011531876.1:p.Glu35Ter
XM_006713097.4:c.103G>T XP_006713160.1:p.Glu35Ter
XM_024453446.1:c.103G>T XP_024309214.1:p.Glu35Ter
NM_001370524.1:c.103G>T NP_001357453.1:p.Glu35Ter
NM_001370525.1:c.103G>T NP_001357454.1:p.Glu35Ter
NM_147196.3:c.262G>T MANE Select NP_671729.2:p.Glu88Ter