Canonical Allele Identifier: CA472429224

Gene: HRAS LRRC56

Linked Data

• ClinVar Variation Id: 1151401
• ClinVar RCV Id: RCV001492334
• dbSNP Id: rs1851272074
• MyVariant Identifiers: chr11:g.533783C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.533783C>T , CM000673.2:g.533783C>T	GRCh38
NC_000011.9:g.533783C>T , CM000673.1:g.533783C>T	GRCh37
NC_000011.8:g.523783C>T	NCBI36
NG_007666.1:g.6768G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000397594.7:c.273G>A (HRAS)	ENSP00000380722.3:p.Glu91=
ENST00000417302.7:c.273G>A (HRAS) MANE Plus Clinical	ENSP00000388246.1:p.Glu91=
ENST00000417302.6:c.273G>A (HRAS)	ENSP00000388246.1:p.Glu91=
ENST00000462734.2:c.273G>A (HRAS)	ENSP00000507303.1:p.Glu91=
ENST00000311189.8:c.273G>A (HRAS) MANE Select	ENSP00000309845.7:p.Glu91=
ENST00000311189.7:c.273G>A (HRAS)	ENSP00000309845.7:p.Glu91=
ENST00000397594.5:c.273G>A (HRAS)	ENSP00000380722.1:p.Glu91=
ENST00000397596.6:c.273G>A (HRAS)	ENSP00000380723.2:p.Glu91=
ENST00000417302.5:c.273G>A (HRAS)	ENSP00000388246.1:p.Glu91=
ENST00000451590.5:c.273G>A (HRAS)	ENSP00000407586.1:p.Glu91=
ENST00000479482.1:n.194G>A (HRAS)
ENST00000493230.5:c.273G>A (HRAS)	ENSP00000434023.1:p.Glu91=
NM_001130442.1:c.273G>A (HRAS)	NP_001123914.1:p.Glu91=
NM_005343.2:c.273G>A (HRAS)	NP_005334.1:p.Glu91=
NM_176795.3:c.273G>A (HRAS)	NP_789765.1:p.Glu91=
XM_011519875.1:c.-424-4815C>T (LRRC56)	XP_011518177.1:n.-424-4815C>T
XM_011519877.1:c.-162+5446C>T (LRRC56)	XP_011518179.1:n.-162+5446C>T
XR_242795.1:n.472G>A (HRAS)
NM_001130442.2:c.273G>A (HRAS)	NP_001123914.1:p.Glu91=
NM_001318054.1:c.-47G>A (HRAS)	NP_001304983.1:n.-47G>A
NM_005343.3:c.273G>A (HRAS)	NP_005334.1:p.Glu91=
NM_176795.4:c.273G>A (HRAS)	NP_789765.1:p.Glu91=
XM_011519875.2:c.-424-4815C>T (LRRC56)	XP_011518177.1:n.-424-4815C>T
XM_011519877.2:c.-162+5446C>T (LRRC56)	XP_011518179.1:n.-162+5446C>T
XM_017017167.1:c.-499-4740C>T (LRRC56)	XP_016872656.1:n.-499-4740C>T
XM_017017168.1:c.-499-4740C>T (LRRC56)	XP_016872657.1:n.-499-4740C>T
NM_005343.4:c.273G>A (HRAS) MANE Select	NP_005334.1:p.Glu91=
NM_001318054.2:c.-47G>A (HRAS)	NP_001304983.1:n.-47G>A
NM_001130442.3:c.273G>A (HRAS)	NP_001123914.1:p.Glu91=
NM_176795.5:c.273G>A (HRAS) MANE Plus Clinical	NP_789765.1:p.Glu91=