Canonical Allele Identifier: CA467493874
Gene: TOR1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.132576458A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129814179A>G , CM000671.2:g.129814179A>G GRCh38
NC_000009.11:g.132576458A>G , CM000671.1:g.132576458A>G GRCh37
NC_000009.10:g.131616279A>G NCBI36
NG_008049.1:g.14984T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000351698.5:c.792T>C MANE Select ENSP00000345719.4:p.Asp264=
ENST00000651202.1:c.*60T>C ENSP00000498222.1:n.*60T>C
ENST00000351698.4:c.792T>C ENSP00000345719.4:p.Asp264=
ENST00000474192.1:n.376T>C
NM_000113.2:c.792T>C NP_000104.1:p.Asp264=
XR_929731.1:n.1119T>C
XR_929731.3:n.987T>C
NM_000113.3:c.792T>C MANE Select NP_000104.1:p.Asp264=