Canonical Allele Identifier: CA410147696

Gene: RUNX1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.34792336G>C , CM000683.2:g.34792336G>C	GRCh38
NC_000021.8:g.36164633G>C , CM000683.1:g.36164633G>C	GRCh37
NC_000021.7:g.35086503G>C	NCBI36
NG_011402.2:g.1197376C>G , LRG_482:g.1197376C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675419.1:c.1242C>G MANE Select	ENSP00000501943.1:p.Tyr414Ter
ENST00000300305.7:c.1242C>G	ENSP00000300305.3:p.Tyr414Ter
ENST00000344691.8:c.1161C>G	ENSP00000340690.4:p.Tyr387Ter
ENST00000399240.5:c.969C>G	ENSP00000382184.1:p.Tyr323Ter
ENST00000437180.5:c.1242C>G	ENSP00000409227.1:p.Tyr414Ter
ENST00000482318.5:c.*832C>G	ENSP00000477067.1:n.*832C>G
NM_001001890.2:c.1161C>G	NP_001001890.1:p.Tyr387Ter
NM_001754.4:c.1242C>G , LRG_482t1:c.1242C>G	NP_001745.2:p.Tyr414Ter
XM_005261068.3:c.1206C>G	XP_005261125.1:p.Tyr402Ter
XM_005261069.3:c.1050C>G	XP_005261126.1:p.Tyr350Ter
XM_011529766.1:c.1242C>G	XP_011528068.1:p.Tyr414Ter
XM_011529767.1:c.1203C>G	XP_011528069.1:p.Tyr401Ter
XM_011529768.1:c.1011C>G	XP_011528070.1:p.Tyr337Ter
XM_005261069.4:c.1050C>G	XP_005261126.1:p.Tyr350Ter
XM_011529766.2:c.1242C>G	XP_011528068.1:p.Tyr414Ter
XM_011529767.2:c.1203C>G	XP_011528069.1:p.Tyr401Ter
XM_011529768.2:c.1011C>G	XP_011528070.1:p.Tyr337Ter
XM_017028487.1:c.1089C>G	XP_016883976.1:p.Tyr363Ter
NM_001001890.3:c.1161C>G	NP_001001890.1:p.Tyr387Ter
NM_001754.5:c.1242C>G MANE Select	NP_001745.2:p.Tyr414Ter