Canonical Allele Identifier: CA2665467506

Gene: TMIE

Linked Data

• gnomAD v4: 3-46709067-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46709067G>T , CM000665.2:g.46709067G>T	GRCh38
NC_000003.11:g.46750557G>T , CM000665.1:g.46750557G>T	GRCh37
NC_000003.10:g.46725561G>T	NCBI36
NG_011628.1:g.12735G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000643606.3:c.212-59G>T MANE Select	ENSP00000494576.2:n.212-59G>T
ENST00000644830.1:c.53-59G>T	ENSP00000495111.1:n.53-59G>T
ENST00000651652.1:c.110-59G>T	ENSP00000498953.1:n.110-59G>T
ENST00000326431.3:c.212-59G>T	ENSP00000324775.3:n.212-59G>T
NM_147196.2:c.212-59G>T	NP_671729.2:n.212-59G>T
XM_006713097.2:c.53-59G>T	XP_006713160.1:n.53-59G>T
XM_011533574.1:c.53-59G>T	XP_011531876.1:n.53-59G>T
XM_006713097.4:c.53-59G>T	XP_006713160.1:n.53-59G>T
XM_024453446.1:c.53-59G>T	XP_024309214.1:n.53-59G>T
NM_001370524.1:c.53-59G>T	NP_001357453.1:n.53-59G>T
NM_001370525.1:c.53-59G>T	NP_001357454.1:n.53-59G>T
NM_147196.3:c.212-59G>T MANE Select	NP_671729.2:n.212-59G>T