Canonical Allele Identifier: CA467493709
Gene: TOR1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.132576347A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129814068A>C , CM000671.2:g.129814068A>C GRCh38
NC_000009.11:g.132576347A>C , CM000671.1:g.132576347A>C GRCh37
NC_000009.10:g.131616168A>C NCBI36
NG_008049.1:g.15095T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000351698.5:c.903T>G MANE Select ENSP00000345719.4:p.Ala301=
ENST00000651202.1:c.*171T>G ENSP00000498222.1:n.*171T>G
ENST00000351698.4:c.903T>G ENSP00000345719.4:p.Ala301=
ENST00000474192.1:n.487T>G
NM_000113.2:c.903T>G NP_000104.1:p.Ala301=
XR_929731.1:n.1230T>G
XR_929731.3:n.1098T>G
NM_000113.3:c.903T>G MANE Select NP_000104.1:p.Ala301=