Canonical Allele Identifier: CA2306830678
Gene: RAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59269064C= , CM000680.2:g.59269064C= GRCh38
NC_000018.9:g.56936296C= , CM000680.1:g.56936296C= GRCh37
NC_000018.8:g.55087276C= NCBI36
NG_013031.1:g.9330G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000334889.4:c.981G= MANE Select ENSP00000334813.3:p.Ala327=
ENST00000256852.7:c.*412G= ENSP00000256852.7:n.*412G=
ENST00000334889.3:c.981G= ENSP00000334813.3:p.Ala327=
NM_013435.2:c.981G= NP_038463.2:p.Ala327=
NM_013435.3:c.981G= MANE Select NP_038463.2:p.Ala327=