Canonical Allele Identifier: CA467493886
Gene: TOR1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.132576467G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129814188G>A , CM000671.2:g.129814188G>A GRCh38
NC_000009.11:g.132576467G>A , CM000671.1:g.132576467G>A GRCh37
NC_000009.10:g.131616288G>A NCBI36
NG_008049.1:g.14975C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000351698.5:c.783C>T MANE Select ENSP00000345719.4:p.Asn261=
ENST00000651202.1:c.*51C>T ENSP00000498222.1:n.*51C>T
ENST00000351698.4:c.783C>T ENSP00000345719.4:p.Asn261=
ENST00000474192.1:n.367C>T
NM_000113.2:c.783C>T NP_000104.1:p.Asn261=
XR_929731.1:n.1110C>T
XR_929731.3:n.978C>T
NM_000113.3:c.783C>T MANE Select NP_000104.1:p.Asn261=
Search 100 bp 5'
Search 100 bp 3'