Canonical Allele Identifier: CA467493906
Gene: TOR1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.132576476A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129814197A>G , CM000671.2:g.129814197A>G GRCh38
NC_000009.11:g.132576476A>G , CM000671.1:g.132576476A>G GRCh37
NC_000009.10:g.131616297A>G NCBI36
NG_008049.1:g.14966T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000351698.5:c.774T>C MANE Select ENSP00000345719.4:p.Ile258=
ENST00000651202.1:c.*42T>C ENSP00000498222.1:n.*42T>C
ENST00000351698.4:c.774T>C ENSP00000345719.4:p.Ile258=
ENST00000474192.1:n.358T>C
NM_000113.2:c.774T>C NP_000104.1:p.Ile258=
XR_929731.1:n.1101T>C
XR_929731.3:n.969T>C
NM_000113.3:c.774T>C MANE Select NP_000104.1:p.Ile258=
Search 100 bp 5'
Search 100 bp 3'