Canonical Allele Identifier: CA2678973926

Gene: RUNX2

Linked Data

• gnomAD v4: 6-45547326-G-GATACCACTGGGCCAC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.45547326_45547327insATACCACTGGGCCAC , CM000668.2:g.45547326_45547327insATACCACTGGGCCAC	GRCh38
NC_000006.11:g.45515063_45515064insATACCACTGGGCCAC , CM000668.1:g.45515063_45515064insATACCACTGGGCCAC	GRCh37
NC_000006.10:g.45623041_45623042insATACCACTGGGCCAC	NCBI36
NG_008020.1:g.224010_224011insATACCACTGGGCCAC
NG_008020.2:g.224010_224011insATACCACTGGGCCAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000646519.1:c.*744_*745insATACCACTGGGCCAC	ENSP00000496517.1:n.*744_*745insATACCACTG...
ENST00000647337.2:c.*21_*22insATACCACTGGGCCAC MANE Select	ENSP00000495497.1:n.*21_*22insATACCACTGGG...
ENST00000359524.7:c.*21_*22insATACCACTGGGCCAC	ENSP00000352514.5:n.*21_*22insATACCACTGGG...
ENST00000371432.7:c.*21_*22insATACCACTGGGCCAC	ENSP00000360486.4:n.*21_*22insATACCACTGGG...
ENST00000371436.10:c.1521_1522insATACCACTGGGCCAC	ENSP00000360491.6:n.1521_1522insATACCACTG...
ENST00000371438.5:c.*21_*22insATACCACTGGGCCAC	ENSP00000360493.1:n.*21_*22insATACCACTGGG...
ENST00000478660.6:c.*178+33673_*178+33674insATACCACTGGGCCAC	ENSP00000460188.1:n.*178+33673_*178+33674...
ENST00000576263.5:c.1021+34919_1021+34920insATACCACTGGGCCAC	ENSP00000458178.1:n.1021+34919_1021+34920...
NM_001015051.3:c.*21_*22insATACCACTGGGCCAC	NP_001015051.3:n.*21_*22insATACCACTGGGCCA...
NM_001024630.3:c.*21_*22insATACCACTGGGCCAC	NP_001019801.3:n.*21_*22insATACCACTGGGCCA...
NM_001278478.1:c.1479_1480insATACCACTGGGCCAC	NP_001265407.1:n.1479_1480insATACCACTGGGC...
XM_006715232.1:c.*21_*22insATACCACTGGGCCAC	XP_006715295.1:n.*21_*22insATACCACTGGGCCA...
XM_011514960.1:c.1225+34919_1225+34920insATACCACTGGGCCAC	XP_011513262.1:n.1225+34919_1225+34920ins...
XM_011514961.1:c.*21_*22insATACCACTGGGCCAC	XP_011513263.1:n.*21_*22insATACCACTGGGCCA...
XM_011514962.1:c.*21_*22insATACCACTGGGCCAC	XP_011513264.1:n.*21_*22insATACCACTGGGCCA...
XM_011514963.1:c.1051+34919_1051+34920insATACCACTGGGCCAC	XP_011513265.1:n.1051+34919_1051+34920ins...
XM_011514964.1:c.1435+356_1435+357insATACCACTGGGCCAC	XP_011513266.1:n.1435+356_1435+357insATAC...
XM_011514966.1:c.553+34919_553+34920insATACCACTGGGCCAC	XP_011513268.1:n.553+34919_553+34920insAT...
NM_001024630.4:c.*21_*22insATACCACTGGGCCAC MANE Select	NP_001019801.3:n.*21_*22insATACCACTGGGCCA...
NM_001278478.2:c.*21_*22insATACCACTGGGCCAC	NP_001265407.1:n.*21_*22insATACCACTGGGCCA...
NM_001369405.1:c.*21_*22insATACCACTGGGCCAC	NP_001356334.1:n.*21_*22insATACCACTGGGCCA...
NM_001015051.4:c.*21_*22insATACCACTGGGCCAC	NP_001015051.3:n.*21_*22insATACCACTGGGCCA...