Canonical Allele Identifier: CA2577575585
Gene: TMIE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46705690A>G , CM000665.2:g.46705690A>G GRCh38
NC_000003.11:g.46747180A>G , CM000665.1:g.46747180A>G GRCh37
NC_000003.10:g.46722184A>G NCBI36
NG_011628.1:g.9358A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000643606.3:c.94-100A>G MANE Select ENSP00000494576.2:n.94-100A>G
ENST00000644830.1:c.-66-100A>G ENSP00000495111.1:n.-66-100A>G
ENST00000326431.3:c.94-100A>G ENSP00000324775.3:n.94-100A>G
NM_147196.2:c.94-100A>G NP_671729.2:n.94-100A>G
XM_006713097.2:c.-66-100A>G XP_006713160.1:n.-66-100A>G
XM_011533574.1:c.-66-100A>G XP_011531876.1:n.-66-100A>G
XM_006713097.4:c.-66-100A>G XP_006713160.1:n.-66-100A>G
XM_024453446.1:c.-66-100A>G XP_024309214.1:n.-66-100A>G
NM_001370524.1:c.-66-100A>G NP_001357453.1:n.-66-100A>G
NM_001370525.1:c.-66-100A>G NP_001357454.1:n.-66-100A>G
NM_147196.3:c.94-100A>G MANE Select NP_671729.2:n.94-100A>G