Canonical Allele Identifier: CA907590224

Gene: TMIE

Linked Data

• dbSNP Id: rs1477183352
• MyVariant Identifiers: chr3:g.46750499del (hg19) ; chr3:g.46709009del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46709011del , CM000665.2:g.46709011del	GRCh38
NC_000003.11:g.46750501del , CM000665.1:g.46750501del	GRCh37
NC_000003.10:g.46725505del	NCBI36
NG_011628.1:g.12679del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643606.3:c.212-115del MANE Select	ENSP00000494576.2:n.212-115del
ENST00000644830.1:c.53-115del	ENSP00000495111.1:n.53-115del
ENST00000651652.1:c.110-115del	ENSP00000498953.1:n.110-115del
ENST00000326431.3:c.212-115del	ENSP00000324775.3:n.212-115del
NM_147196.2:c.212-115del	NP_671729.2:n.212-115del
XM_006713097.2:c.53-115del	XP_006713160.1:n.53-115del
XM_011533574.1:c.53-115del	XP_011531876.1:n.53-115del
XM_006713097.4:c.53-115del	XP_006713160.1:n.53-115del
XM_024453446.1:c.53-115del	XP_024309214.1:n.53-115del
NM_001370524.1:c.53-115del	NP_001357453.1:n.53-115del
NM_001370525.1:c.53-115del	NP_001357454.1:n.53-115del
NM_147196.3:c.212-115del MANE Select	NP_671729.2:n.212-115del