Canonical Allele Identifier: CA2523648440

Gene: TMIE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46706052_46706053insG , CM000665.2:g.46706052_46706053insG	GRCh38
NC_000003.11:g.46747542_46747543insG , CM000665.1:g.46747542_46747543insG	GRCh37
NC_000003.10:g.46722546_46722547insG	NCBI36
NG_011628.1:g.9720_9721insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643606.3:c.211+145_211+146insG MANE Select	ENSP00000494576.2:n.211+145_211+146insG
ENST00000644830.1:c.52+145_52+146insG	ENSP00000495111.1:n.52+145_52+146insG
ENST00000651652.1:c.109+145_109+146insG	ENSP00000498953.1:n.109+145_109+146insG
ENST00000326431.3:c.211+145_211+146insG	ENSP00000324775.3:n.211+145_211+146insG
NM_147196.2:c.211+145_211+146insG	NP_671729.2:n.211+145_211+146insG
XM_006713097.2:c.52+145_52+146insG	XP_006713160.1:n.52+145_52+146insG
XM_011533574.1:c.52+145_52+146insG	XP_011531876.1:n.52+145_52+146insG
XM_006713097.4:c.52+145_52+146insG	XP_006713160.1:n.52+145_52+146insG
XM_024453446.1:c.52+145_52+146insG	XP_024309214.1:n.52+145_52+146insG
NM_001370524.1:c.52+145_52+146insG	NP_001357453.1:n.52+145_52+146insG
NM_001370525.1:c.52+145_52+146insG	NP_001357454.1:n.52+145_52+146insG
NM_147196.3:c.211+145_211+146insG MANE Select	NP_671729.2:n.211+145_211+146insG