Canonical Allele Identifier: CA1362233316

Gene: TMIE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46706257_46706258delinsAC , CM000665.2:g.46706257_46706258delinsAC	GRCh38
NC_000003.11:g.46747747_46747748delinsAC , CM000665.1:g.46747747_46747748delinsAC	GRCh37
NC_000003.10:g.46722751_46722752delinsAC	NCBI36
NG_011628.1:g.9925_9926delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643606.3:c.211+350_211+351delinsAC MANE Select	ENSP00000494576.2:n.211+350_211+351delinsAC
ENST00000644830.1:c.52+350_52+351delinsAC	ENSP00000495111.1:n.52+350_52+351delinsAC
ENST00000651652.1:c.109+350_109+351delinsAC	ENSP00000498953.1:n.109+350_109+351delinsAC
ENST00000326431.3:c.211+350_211+351delinsAC	ENSP00000324775.3:n.211+350_211+351delinsAC
NM_147196.2:c.211+350_211+351delinsAC	NP_671729.2:n.211+350_211+351delinsAC
XM_006713097.2:c.52+350_52+351delinsAC	XP_006713160.1:n.52+350_52+351delinsAC
XM_011533574.1:c.52+350_52+351delinsAC	XP_011531876.1:n.52+350_52+351delinsAC
XM_006713097.4:c.52+350_52+351delinsAC	XP_006713160.1:n.52+350_52+351delinsAC
XM_024453446.1:c.52+350_52+351delinsAC	XP_024309214.1:n.52+350_52+351delinsAC
NM_001370524.1:c.52+350_52+351delinsAC	NP_001357453.1:n.52+350_52+351delinsAC
NM_001370525.1:c.52+350_52+351delinsAC	NP_001357454.1:n.52+350_52+351delinsAC
NM_147196.3:c.211+350_211+351delinsAC MANE Select	NP_671729.2:n.211+350_211+351delinsAC