Canonical Allele Identifier: CA73730631
Gene: TMIE HGNC NCBI

Linked Data

dbSNP Id: rs961229183
MyVariant Identifiers: chr3:g.46747639_46747640insT (hg19) chr3:g.46706149_46706150insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46706151dup , CM000665.2:g.46706151dup GRCh38
NC_000003.11:g.46747641dup , CM000665.1:g.46747641dup GRCh37
NC_000003.10:g.46722645dup NCBI36
NG_011628.1:g.9819dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000643606.3:c.211+244dup MANE Select ENSP00000494576.2:n.211+244dup
ENST00000644830.1:c.52+244dup ENSP00000495111.1:n.52+244dup
ENST00000651652.1:c.109+244dup ENSP00000498953.1:n.109+244dup
ENST00000326431.3:c.211+244dup ENSP00000324775.3:n.211+244dup
NM_147196.2:c.211+244dup NP_671729.2:n.211+244dup
XM_006713097.2:c.52+244dup XP_006713160.1:n.52+244dup
XM_011533574.1:c.52+244dup XP_011531876.1:n.52+244dup
XM_006713097.4:c.52+244dup XP_006713160.1:n.52+244dup
XM_024453446.1:c.52+244dup XP_024309214.1:n.52+244dup
NM_001370524.1:c.52+244dup NP_001357453.1:n.52+244dup
NM_001370525.1:c.52+244dup NP_001357454.1:n.52+244dup
NM_147196.3:c.211+244dup MANE Select NP_671729.2:n.211+244dup
Search 100 bp 5'
Search 100 bp 3'