Canonical Allele Identifier: CA2573147056

Gene: HRAS LRRC56

Linked Data

• ClinVar Variation Id: 1478514
• ClinVar RCV Id: RCV001974222
• dbSNP Id: rs2133990973

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.533874_533888dup , CM000673.2:g.533874_533888dup	GRCh38
NC_000011.9:g.533874_533888dup , CM000673.1:g.533874_533888dup	GRCh37
NC_000011.8:g.523874_523888dup	NCBI36
NG_007666.1:g.6666_6680dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397594.7:c.171_185dup (HRAS)	ENSP00000380722.3:p.Gln61_Glu62insAspThrAlaGlyGln
ENST00000417302.7:c.171_185dup (HRAS) MANE Plus Clinical	ENSP00000388246.1:p.Gln61_Glu62insAspThrAlaGlyGln
ENST00000417302.6:c.171_185dup (HRAS)	ENSP00000388246.1:p.Gln61_Glu62insAspThrAlaGlyGln
ENST00000462734.2:c.171_185dup (HRAS)	ENSP00000507303.1:p.Gln61_Glu62insAspThrAlaGlyGln
ENST00000311189.8:c.171_185dup (HRAS) MANE Select	ENSP00000309845.7:p.Gln61_Glu62insAspThrAlaGlyGln
ENST00000311189.7:c.171_185dup (HRAS)	ENSP00000309845.7:p.Gln61_Glu62insAspThrAlaGlyGln
ENST00000397594.5:c.171_185dup (HRAS)	ENSP00000380722.1:p.Gln61_Glu62insAspThrAlaGlyGln
ENST00000397596.6:c.171_185dup (HRAS)	ENSP00000380723.2:p.Gln61_Glu62insAspThrAlaGlyGln
ENST00000417302.5:c.171_185dup (HRAS)	ENSP00000388246.1:p.Gln61_Glu62insAspThrAlaGlyGln
ENST00000451590.5:c.171_185dup (HRAS)	ENSP00000407586.1:p.Gln61_Glu62insAspThrAlaGlyGln
ENST00000468682.2:n.659_673dup (HRAS)
ENST00000479482.1:n.92_106dup (HRAS)
ENST00000493230.5:c.171_185dup (HRAS)	ENSP00000434023.1:p.Gln61_Glu62insAspThrAlaGlyGln
NM_001130442.1:c.171_185dup (HRAS)	NP_001123914.1:p.Gln61_Glu62insAspThrAlaGlyGln
NM_005343.2:c.171_185dup (HRAS)	NP_005334.1:p.Gln61_Glu62insAspThrAlaGlyGln
NM_176795.3:c.171_185dup (HRAS)	NP_789765.1:p.Gln61_Glu62insAspThrAlaGlyGln
XM_011519875.1:c.-424-4724_-424-4710dup (LRRC56)	XP_011518177.1:n.-424-4724_-424-4710dup
XM_011519877.1:c.-162+5537_-162+5551dup (LRRC56)	XP_011518179.1:n.-162+5537_-162+5551dup
XR_242795.1:n.370_384dup (HRAS)
NM_001130442.2:c.171_185dup (HRAS)	NP_001123914.1:p.Gln61_Glu62insAspThrAlaGlyGln
NM_001318054.1:c.-149_-135dup (HRAS)	NP_001304983.1:n.-149_-135dup
NM_005343.3:c.171_185dup (HRAS)	NP_005334.1:p.Gln61_Glu62insAspThrAlaGlyGln
NM_176795.4:c.171_185dup (HRAS)	NP_789765.1:p.Gln61_Glu62insAspThrAlaGlyGln
XM_011519875.2:c.-424-4724_-424-4710dup (LRRC56)	XP_011518177.1:n.-424-4724_-424-4710dup
XM_011519877.2:c.-162+5537_-162+5551dup (LRRC56)	XP_011518179.1:n.-162+5537_-162+5551dup
XM_017017167.1:c.-499-4649_-499-4635dup (LRRC56)	XP_016872656.1:n.-499-4649_-499-4635dup
XM_017017168.1:c.-499-4649_-499-4635dup (LRRC56)	XP_016872657.1:n.-499-4649_-499-4635dup
NM_005343.4:c.171_185dup (HRAS) MANE Select	NP_005334.1:p.Gln61_Glu62insAspThrAlaGlyGln
NM_001318054.2:c.-149_-135dup (HRAS)	NP_001304983.1:n.-149_-135dup
NM_001130442.3:c.171_185dup (HRAS)	NP_001123914.1:p.Gln61_Glu62insAspThrAlaGlyGln
NM_176795.5:c.171_185dup (HRAS) MANE Plus Clinical	NP_789765.1:p.Gln61_Glu62insAspThrAlaGlyGln