Canonical Allele Identifier: CA467493690
Gene: TOR1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.132576308G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129814029G>A , CM000671.2:g.129814029G>A GRCh38
NC_000009.11:g.132576308G>A , CM000671.1:g.132576308G>A GRCh37
NC_000009.10:g.131616129G>A NCBI36
NG_008049.1:g.15134C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000351698.5:c.942C>T MANE Select ENSP00000345719.4:p.Phe314=
ENST00000651202.1:c.*210C>T ENSP00000498222.1:n.*210C>T
ENST00000351698.4:c.942C>T ENSP00000345719.4:p.Phe314=
ENST00000474192.1:n.526C>T
NM_000113.2:c.942C>T NP_000104.1:p.Phe314=
XR_929731.3:n.1137C>T
NM_000113.3:c.942C>T MANE Select NP_000104.1:p.Phe314=