Canonical Allele Identifier: CA375198119
Gene: TOR1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.132576495A>T (hg19) chr9:g.129814216A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129814216A>T , CM000671.2:g.129814216A>T GRCh38
NC_000009.11:g.132576495A>T , CM000671.1:g.132576495A>T GRCh37
NC_000009.10:g.131616316A>T NCBI36
NG_008049.1:g.14947T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000351698.5:c.755T>A MANE Select ENSP00000345719.4:p.Phe252Tyr
ENST00000651202.1:c.*23T>A ENSP00000498222.1:n.*23T>A
ENST00000351698.4:c.755T>A ENSP00000345719.4:p.Phe252Tyr
ENST00000474192.1:n.339T>A
NM_000113.2:c.755T>A NP_000104.1:p.Phe252Tyr
XR_929731.1:n.1082T>A
XR_929731.3:n.950T>A
NM_000113.3:c.755T>A MANE Select NP_000104.1:p.Phe252Tyr
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