Canonical Allele Identifier: CA2611691485

Gene: HRAS LRRC56

Linked Data

• gnomAD v4: 11-533876-G-GGTCACTCGCCCCTTACCTCTGCAGGAGTT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.533876_533877insGTCACTCGCCCCTTACCTCTGCAGGAGTT , CM000673.2:g.533876_533877insGTCACTCGCCCCTTACCTCTGCAGGAGTT	GRCh38
NC_000011.9:g.533876_533877insGTCACTCGCCCCTTACCTCTGCAGGAGTT , CM000673.1:g.533876_533877insGTCACTCGCCCCTTACCTCTGCAGGAGTT	GRCh37
NC_000011.8:g.523876_523877insGTCACTCGCCCCTTACCTCTGCAGGAGTT	NCBI36
NG_007666.1:g.6674_6675insAACTCCTGCAGAGGTAAGGGGCGAGTGAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000397594.7:c.179_180insAACTCCTGCAGAGGTAAGGGGCGAGTGAC (HRAS)	ENSP00000380722.3:p.Gln61ThrfsTer9
ENST00000417302.7:c.179_180insAACTCCTGCAGAGGTAAGGGGCGAGTGAC (HRAS) MANE Plus Clinical	ENSP00000388246.1:p.Gln61ThrfsTer9
ENST00000417302.6:c.179_180insAACTCCTGCAGAGGTAAGGGGCGAGTGAC (HRAS)	ENSP00000388246.1:p.Gln61ThrfsTer9
ENST00000462734.2:c.179_180insAACTCCTGCAGAGGTAAGGGGCGAGTGAC (HRAS)	ENSP00000507303.1:p.Gln61ThrfsTer9
ENST00000311189.8:c.179_180insAACTCCTGCAGAGGTAAGGGGCGAGTGAC (HRAS) MANE Select	ENSP00000309845.7:p.Gln61ThrfsTer9
ENST00000311189.7:c.179_180insAACTCCTGCAGAGGTAAGGGGCGAGTGAC (HRAS)	ENSP00000309845.7:p.Gln61ThrfsTer9
ENST00000397594.5:c.179_180insAACTCCTGCAGAGGTAAGGGGCGAGTGAC (HRAS)	ENSP00000380722.1:p.Gln61ThrfsTer9
ENST00000397596.6:c.179_180insAACTCCTGCAGAGGTAAGGGGCGAGTGAC (HRAS)	ENSP00000380723.2:p.Gln61ThrfsTer9
ENST00000417302.5:c.179_180insAACTCCTGCAGAGGTAAGGGGCGAGTGAC (HRAS)	ENSP00000388246.1:p.Gln61ThrfsTer9
ENST00000451590.5:c.179_180insAACTCCTGCAGAGGTAAGGGGCGAGTGAC (HRAS)	ENSP00000407586.1:p.Gln61ThrfsTer9
ENST00000468682.2:n.667_668insAACTCCTGCAGAGGTAAGGGGCGAGTGAC (HRAS)
ENST00000479482.1:n.100_101insAACTCCTGCAGAGGTAAGGGGCGAGTGAC (HRAS)
ENST00000493230.5:c.179_180insAACTCCTGCAGAGGTAAGGGGCGAGTGAC (HRAS)	ENSP00000434023.1:p.Gln61ThrfsTer9
NM_001130442.1:c.179_180insAACTCCTGCAGAGGTAAGGGGCGAGTGAC (HRAS)	NP_001123914.1:p.Gln61ThrfsTer9
NM_005343.2:c.179_180insAACTCCTGCAGAGGTAAGGGGCGAGTGAC (HRAS)	NP_005334.1:p.Gln61ThrfsTer9
NM_176795.3:c.179_180insAACTCCTGCAGAGGTAAGGGGCGAGTGAC (HRAS)	NP_789765.1:p.Gln61ThrfsTer9
XM_011519875.1:c.-424-4722_-424-4721insGTCACTCGCCCCTTACCTCTGCAGGAGTT (LRRC56)	XP_011518177.1:n.-424-4722_-424-4721insGTCACTCGCCCCTTACCTCTGC...
XM_011519877.1:c.-162+5539_-162+5540insGTCACTCGCCCCTTACCTCTGCAGGAGTT (LRRC56)	XP_011518179.1:n.-162+5539_-162+5540insGTCACTCGCCCCTTACCTCTGC...
XR_242795.1:n.378_379insAACTCCTGCAGAGGTAAGGGGCGAGTGAC (HRAS)
NM_001130442.2:c.179_180insAACTCCTGCAGAGGTAAGGGGCGAGTGAC (HRAS)	NP_001123914.1:p.Gln61ThrfsTer9
NM_001318054.1:c.-141_-140insAACTCCTGCAGAGGTAAGGGGCGAGTGAC (HRAS)	NP_001304983.1:n.-141_-140insAACTCCTGCAGAGGTAAGGGGCGAGTGAC
NM_005343.3:c.179_180insAACTCCTGCAGAGGTAAGGGGCGAGTGAC (HRAS)	NP_005334.1:p.Gln61ThrfsTer9
NM_176795.4:c.179_180insAACTCCTGCAGAGGTAAGGGGCGAGTGAC (HRAS)	NP_789765.1:p.Gln61ThrfsTer9
XM_011519875.2:c.-424-4722_-424-4721insGTCACTCGCCCCTTACCTCTGCAGGAGTT (LRRC56)	XP_011518177.1:n.-424-4722_-424-4721insGTCACTCGCCCCTTACCTCTGC...
XM_011519877.2:c.-162+5539_-162+5540insGTCACTCGCCCCTTACCTCTGCAGGAGTT (LRRC56)	XP_011518179.1:n.-162+5539_-162+5540insGTCACTCGCCCCTTACCTCTGC...
XM_017017167.1:c.-499-4647_-499-4646insGTCACTCGCCCCTTACCTCTGCAGGAGTT (LRRC56)	XP_016872656.1:n.-499-4647_-499-4646insGTCACTCGCCCCTTACCTCTGC...
XM_017017168.1:c.-499-4647_-499-4646insGTCACTCGCCCCTTACCTCTGCAGGAGTT (LRRC56)	XP_016872657.1:n.-499-4647_-499-4646insGTCACTCGCCCCTTACCTCTGC...
NM_005343.4:c.179_180insAACTCCTGCAGAGGTAAGGGGCGAGTGAC (HRAS) MANE Select	NP_005334.1:p.Gln61ThrfsTer9
NM_001318054.2:c.-141_-140insAACTCCTGCAGAGGTAAGGGGCGAGTGAC (HRAS)	NP_001304983.1:n.-141_-140insAACTCCTGCAGAGGTAAGGGGCGAGTGAC
NM_001130442.3:c.179_180insAACTCCTGCAGAGGTAAGGGGCGAGTGAC (HRAS)	NP_001123914.1:p.Gln61ThrfsTer9
NM_176795.5:c.179_180insAACTCCTGCAGAGGTAAGGGGCGAGTGAC (HRAS) MANE Plus Clinical	NP_789765.1:p.Gln61ThrfsTer9