Canonical Allele Identifier: CA467493779
Gene: TOR1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.132576407G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129814128G>T , CM000671.2:g.129814128G>T GRCh38
NC_000009.11:g.132576407G>T , CM000671.1:g.132576407G>T GRCh37
NC_000009.10:g.131616228G>T NCBI36
NG_008049.1:g.15035C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000351698.5:c.843C>A MANE Select ENSP00000345719.4:p.Ile281=
ENST00000651202.1:c.*111C>A ENSP00000498222.1:n.*111C>A
ENST00000351698.4:c.843C>A ENSP00000345719.4:p.Ile281=
ENST00000474192.1:n.427C>A
NM_000113.2:c.843C>A NP_000104.1:p.Ile281=
XR_929731.1:n.1170C>A
XR_929731.3:n.1038C>A
NM_000113.3:c.843C>A MANE Select NP_000104.1:p.Ile281=