Canonical Allele Identifier: CA433458708

Gene: TMIE

Linked Data

• MyVariant Identifiers: chr3:g.46747396C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46705906C>A , CM000665.2:g.46705906C>A	GRCh38
NC_000003.11:g.46747396C>A , CM000665.1:g.46747396C>A	GRCh37
NC_000003.10:g.46722400C>A	NCBI36
NG_011628.1:g.9574C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643606.3:c.210C>A MANE Select	ENSP00000494576.2:p.Ile70=
ENST00000644830.1:c.51C>A	ENSP00000495111.1:p.Ile17=
ENST00000651652.1:c.108C>A	ENSP00000498953.1:p.Ile36=
ENST00000326431.3:c.210C>A	ENSP00000324775.3:p.Ile70=
NM_147196.2:c.210C>A	NP_671729.2:p.Ile70=
XM_006713097.2:c.51C>A	XP_006713160.1:p.Ile17=
XM_011533574.1:c.51C>A	XP_011531876.1:p.Ile17=
XM_006713097.4:c.51C>A	XP_006713160.1:p.Ile17=
XM_024453446.1:c.51C>A	XP_024309214.1:p.Ile17=
NM_001370524.1:c.51C>A	NP_001357453.1:p.Ile17=
NM_001370525.1:c.51C>A	NP_001357454.1:p.Ile17=
NM_147196.3:c.210C>A MANE Select	NP_671729.2:p.Ile70=