Canonical Allele Identifier: CA521691598

Gene: RUNX3

Linked Data

• gnomAD v2: 1-25251804-T-TCCCCCCCCCCC
• gnomAD v3: 1-24925313-T-TCCCCCCCCCCC
• gnomAD v4: 1-24925313-T-TCCCCCCCCCCC
• MyVariant Identifiers: chr1:g.25251804_25251805insCCCCCCCCCCC (hg19) ; chr1:g.24925313_24925314insCCCCCCCCCCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.24925318_24925319insCCCCCCCCCCC , CM000663.2:g.24925318_24925319insCCCCCCCCCCC	GRCh38
NC_000001.10:g.25251809_25251810insCCCCCCCCCCC , CM000663.1:g.25251809_25251810insCCCCCCCCCCC	GRCh37
NC_000001.9:g.25124396_25124397insCCCCCCCCCCC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338888.4:c.481+2260_481+2261insGGGGGGGGGGG	ENSP00000343477.3:n.481+2260_481+2261insGGGGGGGGGGG
ENST00000308873.11:c.439+2260_439+2261insGGGGGGGGGGG MANE Select	ENSP00000308051.6:n.439+2260_439+2261insGGGGGGGGGGG
ENST00000308873.10:c.439+2260_439+2261insGGGGGGGGGGG	ENSP00000308051.6:n.439+2260_439+2261insGGGGGGGGGGG
ENST00000338888.3:c.481+2260_481+2261insGGGGGGGGGGG	ENSP00000343477.3:n.481+2260_481+2261insGGGGGGGGGGG
ENST00000399916.5:c.481+2260_481+2261insGGGGGGGGGGG	ENSP00000382800.1:n.481+2260_481+2261insGGGGGGGGGGG
ENST00000496967.1:n.213+2260_213+2261insGGGGGGGGGGG
NM_001031680.2:c.481+2260_481+2261insGGGGGGGGGGG	NP_001026850.1:n.481+2260_481+2261insGGGGGGGGGGG
NM_004350.2:c.439+2260_439+2261insGGGGGGGGGGG	NP_004341.1:n.439+2260_439+2261insGGGGGGGGGGG
XM_005246024.3:c.481+2260_481+2261insGGGGGGGGGGG	XP_005246081.1:n.481+2260_481+2261insGGGGGGGGGGG
XM_011542351.1:c.481+2260_481+2261insGGGGGGGGGGG	XP_011540653.1:n.481+2260_481+2261insGGGGGGGGGGG
NM_001320672.1:c.481+2260_481+2261insGGGGGGGGGGG	NP_001307601.1:n.481+2260_481+2261insGGGGGGGGGGG
XM_005246024.4:c.481+2260_481+2261insGGGGGGGGGGG	XP_005246081.1:n.481+2260_481+2261insGGGGGGGGGGG
XR_001737942.1:n.990_991insCCCCCCCCCCC
NM_004350.3:c.439+2260_439+2261insGGGGGGGGGGG MANE Select	NP_004341.1:n.439+2260_439+2261insGGGGGGGGGGG