Canonical Allele Identifier: CA1362233090
Gene: TMIE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46705793A= , CM000665.2:g.46705793A= GRCh38
NC_000003.11:g.46747283A= , CM000665.1:g.46747283A= GRCh37
NC_000003.10:g.46722287A= NCBI36
NG_011628.1:g.9461A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000643606.3:c.97A= MANE Select ENSP00000494576.2:p.Ser33=
ENST00000644830.1:c.-63A= ENSP00000495111.1:n.-63A=
ENST00000326431.3:c.97A= ENSP00000324775.3:p.Ser33=
NM_147196.2:c.97A= NP_671729.2:p.Ser33=
XM_006713097.2:c.-63A= XP_006713160.1:n.-63A=
XM_011533574.1:c.-63A= XP_011531876.1:n.-63A=
XM_006713097.4:c.-63A= XP_006713160.1:n.-63A=
XM_024453446.1:c.-63A= XP_024309214.1:n.-63A=
NM_001370524.1:c.-63A= NP_001357453.1:n.-63A=
NM_001370525.1:c.-63A= NP_001357454.1:n.-63A=
NM_147196.3:c.97A= MANE Select NP_671729.2:p.Ser33=