Canonical Allele Identifier: CA1880979032
Gene: TOR1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129819098C= , CM000671.2:g.129819098C= GRCh38
NC_000009.11:g.132581377C= , CM000671.1:g.132581377C= GRCh37
NC_000009.10:g.131621198C= NCBI36
NG_008049.1:g.10065G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000351698.5:c.445-178G= MANE Select ENSP00000345719.4:n.445-178G=
ENST00000651202.1:c.541-178G= ENSP00000498222.1:n.541-178G=
ENST00000351698.4:c.445-178G= ENSP00000345719.4:n.445-178G=
ENST00000473604.2:n.555-178G=
NM_000113.2:c.445-178G= NP_000104.1:n.445-178G=
XR_929731.1:n.605-178G=
XR_929731.3:n.473-178G=
NM_000113.3:c.445-178G= MANE Select NP_000104.1:n.445-178G=