Canonical Allele Identifier: CA375199052
Gene: TOR1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.132581037A>G (hg19) chr9:g.129818758A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129818758A>G , CM000671.2:g.129818758A>G GRCh38
NC_000009.11:g.132581037A>G , CM000671.1:g.132581037A>G GRCh37
NC_000009.10:g.131620858A>G NCBI36
NG_008049.1:g.10405T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000351698.5:c.607T>C MANE Select ENSP00000345719.4:p.Phe203Leu
ENST00000651202.1:c.703T>C ENSP00000498222.1:p.Phe235Leu
ENST00000351698.4:c.607T>C ENSP00000345719.4:p.Phe203Leu
ENST00000473604.2:n.717T>C
ENST00000474192.1:n.24T>C
NM_000113.2:c.607T>C NP_000104.1:p.Phe203Leu
XR_929731.1:n.767T>C
XR_929731.3:n.635T>C
NM_000113.3:c.607T>C MANE Select NP_000104.1:p.Phe203Leu
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