Canonical Allele Identifier: CA10629120
Gene: TOR1A HGNC NCBI

Linked Data

ClinVar Variation Id: 365226
ClinVar RCV Id: RCV000384578
dbSNP Id: rs886063521

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129813627G>A , CM000671.2:g.129813627G>A GRCh38
NC_000009.11:g.132575906G>A , CM000671.1:g.132575906G>A GRCh37
NC_000009.10:g.131615727G>A NCBI36
NG_008049.1:g.15536C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000351698.5:c.*345C>T MANE Select ENSP00000345719.4:n.*345C>T
ENST00000651202.1:c.*612C>T ENSP00000498222.1:n.*612C>T
ENST00000351698.4:c.*345C>T ENSP00000345719.4:n.*345C>T
ENST00000474192.1:n.928C>T
NM_000113.2:c.*345C>T NP_000104.1:n.*345C>T
XR_929731.3:n.1539C>T
NM_000113.3:c.*345C>T MANE Select NP_000104.1:n.*345C>T