Canonical Allele Identifier: CA259682

Gene: HRAS LRRC56

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.534212_534214dup , CM000673.2:g.534212_534214dup	GRCh38
NC_000011.9:g.534212_534214dup , CM000673.1:g.534212_534214dup	GRCh37
NC_000011.8:g.524212_524214dup	NCBI36
NG_007666.1:g.6338_6340dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397594.7:c.110_111+1dup (HRAS)
ENST00000417302.7:c.110_111+1dup (HRAS)
ENST00000417302.6:c.110_111+1dup (HRAS)
ENST00000462734.2:c.110_111+1dup (HRAS)
ENST00000311189.8:c.110_111+1dup (HRAS)
ENST00000311189.7:c.110_111+1dup (HRAS)
ENST00000397594.5:c.110_111+1dup (HRAS)
ENST00000397596.6:c.110_111+1dup (HRAS)
ENST00000417302.5:c.110_111+1dup (HRAS)
ENST00000451590.5:c.110_111+1dup (HRAS)
ENST00000468682.2:n.598_599+1dup (HRAS)
ENST00000493230.5:c.110_111+1dup (HRAS)
NM_001130442.1:c.110_111+1dup (HRAS)
NM_005343.2:c.110_111+1dup (HRAS)
NM_176795.3:c.110_111+1dup (HRAS)
XM_011519875.1:c.-424-4386_-424-4384dup (LRRC56)	XP_011518177.1:n.-424-4386_-424-4384dup
XM_011519877.1:c.-161-5368_-161-5366dup (LRRC56)	XP_011518179.1:n.-161-5368_-161-5366dup
XR_242795.1:n.309_310+1dup (HRAS)
NM_001130442.2:c.110_111+1dup (HRAS)
NM_001318054.1:c.-210_-209+1dup (HRAS)
NM_005343.3:c.110_111+1dup (HRAS)
NM_176795.4:c.110_111+1dup (HRAS)
XM_011519875.2:c.-424-4386_-424-4384dup (LRRC56)	XP_011518177.1:n.-424-4386_-424-4384dup
XM_011519877.2:c.-161-5368_-161-5366dup (LRRC56)	XP_011518179.1:n.-161-5368_-161-5366dup
XM_017017167.1:c.-499-4311_-499-4309dup (LRRC56)	XP_016872656.1:n.-499-4311_-499-4309dup
XM_017017168.1:c.-499-4311_-499-4309dup (LRRC56)	XP_016872657.1:n.-499-4311_-499-4309dup
NM_005343.4:c.110_111+1dup (HRAS)
NM_001318054.2:c.-210_-209+1dup (HRAS)
NM_001130442.3:c.110_111+1dup (HRAS)
NM_176795.5:c.110_111+1dup (HRAS)