Canonical Allele Identifier: CA1362234489

Gene: TMIE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46709008_46709009delinsAG , CM000665.2:g.46709008_46709009delinsAG	GRCh38
NC_000003.11:g.46750498_46750499delinsAG , CM000665.1:g.46750498_46750499delinsAG	GRCh37
NC_000003.10:g.46725502_46725503delinsAG	NCBI36
NG_011628.1:g.12676_12677delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643606.3:c.212-118_212-117delinsAG MANE Select	ENSP00000494576.2:n.212-118_212-117delinsAG
ENST00000644830.1:c.53-118_53-117delinsAG	ENSP00000495111.1:n.53-118_53-117delinsAG
ENST00000651652.1:c.110-118_110-117delinsAG	ENSP00000498953.1:n.110-118_110-117delinsAG
ENST00000326431.3:c.212-118_212-117delinsAG	ENSP00000324775.3:n.212-118_212-117delinsAG
NM_147196.2:c.212-118_212-117delinsAG	NP_671729.2:n.212-118_212-117delinsAG
XM_006713097.2:c.53-118_53-117delinsAG	XP_006713160.1:n.53-118_53-117delinsAG
XM_011533574.1:c.53-118_53-117delinsAG	XP_011531876.1:n.53-118_53-117delinsAG
XM_006713097.4:c.53-118_53-117delinsAG	XP_006713160.1:n.53-118_53-117delinsAG
XM_024453446.1:c.53-118_53-117delinsAG	XP_024309214.1:n.53-118_53-117delinsAG
NM_001370524.1:c.53-118_53-117delinsAG	NP_001357453.1:n.53-118_53-117delinsAG
NM_001370525.1:c.53-118_53-117delinsAG	NP_001357454.1:n.53-118_53-117delinsAG
NM_147196.3:c.212-118_212-117delinsAG MANE Select	NP_671729.2:n.212-118_212-117delinsAG