Canonical Allele Identifier: CA2665467330
Gene: TMIE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46705943_46705944insTGTGTTCCCACTGC , CM000665.2:g.46705943_46705944insTGTGTTCCCACTGC GRCh38
NC_000003.11:g.46747433_46747434insTGTGTTCCCACTGC , CM000665.1:g.46747433_46747434insTGTGTTCCCACTGC GRCh37
NC_000003.10:g.46722437_46722438insTGTGTTCCCACTGC NCBI36
NG_011628.1:g.9611_9612insTGTGTTCCCACTGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000643606.3:c.211+36_211+37insTGTGTTCCCACTGC MANE Select ENSP00000494576.2:n.211+36_211+37insTGTGTTCCCACTGC
ENST00000644830.1:c.52+36_52+37insTGTGTTCCCACTGC ENSP00000495111.1:n.52+36_52+37insTGTGTTCCCACTGC
ENST00000651652.1:c.109+36_109+37insTGTGTTCCCACTGC ENSP00000498953.1:n.109+36_109+37insTGTGTTCCCACTGC
ENST00000326431.3:c.211+36_211+37insTGTGTTCCCACTGC ENSP00000324775.3:n.211+36_211+37insTGTGTTCCCACTGC
NM_147196.2:c.211+36_211+37insTGTGTTCCCACTGC NP_671729.2:n.211+36_211+37insTGTGTTCCCACTGC
XM_006713097.2:c.52+36_52+37insTGTGTTCCCACTGC XP_006713160.1:n.52+36_52+37insTGTGTTCCCACTGC
XM_011533574.1:c.52+36_52+37insTGTGTTCCCACTGC XP_011531876.1:n.52+36_52+37insTGTGTTCCCACTGC
XM_006713097.4:c.52+36_52+37insTGTGTTCCCACTGC XP_006713160.1:n.52+36_52+37insTGTGTTCCCACTGC
XM_024453446.1:c.52+36_52+37insTGTGTTCCCACTGC XP_024309214.1:n.52+36_52+37insTGTGTTCCCACTGC
NM_001370524.1:c.52+36_52+37insTGTGTTCCCACTGC NP_001357453.1:n.52+36_52+37insTGTGTTCCCACTGC
NM_001370525.1:c.52+36_52+37insTGTGTTCCCACTGC NP_001357454.1:n.52+36_52+37insTGTGTTCCCACTGC
NM_147196.3:c.211+36_211+37insTGTGTTCCCACTGC MANE Select NP_671729.2:n.211+36_211+37insTGTGTTCCCACTGC