Canonical Allele Identifier: CA352479313

Gene: TMIE

Linked Data

• MyVariant Identifiers: chr3:g.46747397A>T (hg19) ; chr3:g.46705907A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46705907A>T , CM000665.2:g.46705907A>T	GRCh38
NC_000003.11:g.46747397A>T , CM000665.1:g.46747397A>T	GRCh37
NC_000003.10:g.46722401A>T	NCBI36
NG_011628.1:g.9575A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643606.3:c.211A>T MANE Select	ENSP00000494576.2:p.Ile71Phe
ENST00000644830.1:c.52A>T	ENSP00000495111.1:p.Ile18Phe
ENST00000651652.1:c.109A>T	ENSP00000498953.1:p.Ile37Phe
ENST00000326431.3:c.211A>T	ENSP00000324775.3:p.Ile71Phe
NM_147196.2:c.211A>T	NP_671729.2:p.Ile71Phe
XM_006713097.2:c.52A>T	XP_006713160.1:p.Ile18Phe
XM_011533574.1:c.52A>T	XP_011531876.1:p.Ile18Phe
XM_006713097.4:c.52A>T	XP_006713160.1:p.Ile18Phe
XM_024453446.1:c.52A>T	XP_024309214.1:p.Ile18Phe
NM_001370524.1:c.52A>T	NP_001357453.1:p.Ile18Phe
NM_001370525.1:c.52A>T	NP_001357454.1:p.Ile18Phe
NM_147196.3:c.211A>T MANE Select	NP_671729.2:p.Ile71Phe