Canonical Allele Identifier: CA375197408
Gene: TOR1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1686266
ClinVar RCV Id: RCV002246779
dbSNP Id: rs2131001171

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129814013T>C , CM000671.2:g.129814013T>C GRCh38
NC_000009.11:g.132576292T>C , CM000671.1:g.132576292T>C GRCh37
NC_000009.10:g.131616113T>C NCBI36
NG_008049.1:g.15150A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000351698.5:c.958A>G MANE Select ENSP00000345719.4:p.Lys320Glu
ENST00000651202.1:c.*226A>G ENSP00000498222.1:n.*226A>G
ENST00000351698.4:c.958A>G ENSP00000345719.4:p.Lys320Glu
ENST00000474192.1:n.542A>G
NM_000113.2:c.958A>G NP_000104.1:p.Lys320Glu
XR_929731.3:n.1153A>G
NM_000113.3:c.958A>G MANE Select NP_000104.1:p.Lys320Glu