Canonical Allele Identifier: CA467493913
Gene: TOR1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.132576479T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129814200T>C , CM000671.2:g.129814200T>C GRCh38
NC_000009.11:g.132576479T>C , CM000671.1:g.132576479T>C GRCh37
NC_000009.10:g.131616300T>C NCBI36
NG_008049.1:g.14963A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000351698.5:c.771A>G MANE Select ENSP00000345719.4:p.Leu257=
ENST00000651202.1:c.*39A>G ENSP00000498222.1:n.*39A>G
ENST00000351698.4:c.771A>G ENSP00000345719.4:p.Leu257=
ENST00000474192.1:n.355A>G
NM_000113.2:c.771A>G NP_000104.1:p.Leu257=
XR_929731.1:n.1098A>G
XR_929731.3:n.966A>G
NM_000113.3:c.771A>G MANE Select NP_000104.1:p.Leu257=