Canonical Allele Identifier: CA433459121

Gene: TMIE

Linked Data

• MyVariant Identifiers: chr3:g.46750662G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46709172G>A , CM000665.2:g.46709172G>A	GRCh38
NC_000003.11:g.46750662G>A , CM000665.1:g.46750662G>A	GRCh37
NC_000003.10:g.46725666G>A	NCBI36
NG_011628.1:g.12840G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643606.3:c.258G>A MANE Select	ENSP00000494576.2:p.Arg86=
ENST00000644830.1:c.99G>A	ENSP00000495111.1:p.Arg33=
ENST00000651652.1:c.156G>A	ENSP00000498953.1:p.Arg52=
ENST00000326431.3:c.258G>A	ENSP00000324775.3:p.Arg86=
NM_147196.2:c.258G>A	NP_671729.2:p.Arg86=
XM_006713097.2:c.99G>A	XP_006713160.1:p.Arg33=
XM_011533574.1:c.99G>A	XP_011531876.1:p.Arg33=
XM_006713097.4:c.99G>A	XP_006713160.1:p.Arg33=
XM_024453446.1:c.99G>A	XP_024309214.1:p.Arg33=
NM_001370524.1:c.99G>A	NP_001357453.1:p.Arg33=
NM_001370525.1:c.99G>A	NP_001357454.1:p.Arg33=
NM_147196.3:c.258G>A MANE Select	NP_671729.2:p.Arg86=