Canonical Allele Identifier: CA375199335
Gene: TOR1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.132581163C>G (hg19) chr9:g.129818884C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129818884C>G , CM000671.2:g.129818884C>G GRCh38
NC_000009.11:g.132581163C>G , CM000671.1:g.132581163C>G GRCh37
NC_000009.10:g.131620984C>G NCBI36
NG_008049.1:g.10279G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000351698.5:c.481G>C MANE Select ENSP00000345719.4:p.Ala161Pro
ENST00000651202.1:c.577G>C ENSP00000498222.1:p.Ala193Pro
ENST00000351698.4:c.481G>C ENSP00000345719.4:p.Ala161Pro
ENST00000473604.2:n.591G>C
NM_000113.2:c.481G>C NP_000104.1:p.Ala161Pro
XR_929731.1:n.641G>C
XR_929731.3:n.509G>C
NM_000113.3:c.481G>C MANE Select NP_000104.1:p.Ala161Pro
Search 100 bp 5'
Search 100 bp 3'