Canonical Allele Identifier: CA10977448

Gene: RUNX3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.24917063C>T , CM000663.2:g.24917063C>T	GRCh38
NC_000001.10:g.25243554C>T , CM000663.1:g.25243554C>T	GRCh37
NC_000001.9:g.25116141C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338888.4:c.586+2177G>A	ENSP00000343477.3:n.586+2177G>A
ENST00000308873.11:c.544+2177G>A MANE Select	ENSP00000308051.6:n.544+2177G>A
ENST00000308873.10:c.544+2177G>A	ENSP00000308051.6:n.544+2177G>A
ENST00000338888.3:c.586+2177G>A	ENSP00000343477.3:n.586+2177G>A
ENST00000399916.5:c.586+2177G>A	ENSP00000382800.1:n.586+2177G>A
ENST00000496967.1:n.318+2177G>A
NM_001031680.2:c.586+2177G>A	NP_001026850.1:n.586+2177G>A
NM_004350.2:c.544+2177G>A	NP_004341.1:n.544+2177G>A
XM_005246024.3:c.586+2177G>A	XP_005246081.1:n.586+2177G>A
XM_011542351.1:c.586+2177G>A	XP_011540653.1:n.586+2177G>A
NM_001320672.1:c.586+2177G>A	NP_001307601.1:n.586+2177G>A
XM_005246024.4:c.586+2177G>A	XP_005246081.1:n.586+2177G>A
NM_004350.3:c.544+2177G>A MANE Select	NP_004341.1:n.544+2177G>A