Canonical Allele Identifier: CA1140105853
Gene: RUNX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.24925450G= , CM000663.2:g.24925450G= GRCh38
NC_000001.10:g.25251941G= , CM000663.1:g.25251941G= GRCh37
NC_000001.9:g.25124528G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000338888.4:c.481+2124C= ENSP00000343477.3:n.481+2124C=
ENST00000308873.11:c.439+2124C= MANE Select ENSP00000308051.6:n.439+2124C=
ENST00000308873.10:c.439+2124C= ENSP00000308051.6:n.439+2124C=
ENST00000338888.3:c.481+2124C= ENSP00000343477.3:n.481+2124C=
ENST00000399916.5:c.481+2124C= ENSP00000382800.1:n.481+2124C=
ENST00000496967.1:n.213+2124C=
NM_001031680.2:c.481+2124C= NP_001026850.1:n.481+2124C=
NM_004350.2:c.439+2124C= NP_004341.1:n.439+2124C=
XM_005246024.3:c.481+2124C= XP_005246081.1:n.481+2124C=
XM_011542351.1:c.481+2124C= XP_011540653.1:n.481+2124C=
NM_001320672.1:c.481+2124C= NP_001307601.1:n.481+2124C=
XM_005246024.4:c.481+2124C= XP_005246081.1:n.481+2124C=
XR_001737942.1:n.1122G=
NM_004350.3:c.439+2124C= MANE Select NP_004341.1:n.439+2124C=