Canonical Allele Identifier: CA2580083844

Gene: HRAS LRRC56

Linked Data

• ClinVar Variation Id: 2044453
• ClinVar RCV Id: RCV002903700

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.533470_533879dup , CM000673.2:g.533470_533879dup	GRCh38
NC_000011.9:g.533470_533879dup , CM000673.1:g.533470_533879dup	GRCh37
NC_000011.8:g.523470_523879dup	NCBI36
NG_007666.1:g.6678_7087dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000397594.7:c.183_439dup (HRAS)
ENST00000417302.7:c.183_439dup (HRAS)
ENST00000417302.6:c.183_439dup (HRAS)
ENST00000462734.2:c.183_439dup (HRAS)
ENST00000311189.8:c.183_439dup (HRAS)
ENST00000311189.7:c.183_439dup (HRAS)
ENST00000397594.5:c.183_439dup (HRAS)
ENST00000397596.6:c.183_439dup (HRAS)
ENST00000417302.5:c.183_439dup (HRAS)
ENST00000451590.5:c.183_439dup (HRAS)
ENST00000479482.1:n.104_360dup (HRAS)
ENST00000493230.5:c.183_439dup (HRAS)
NM_001130442.1:c.183_439dup (HRAS)
NM_005343.2:c.183_439dup (HRAS)
NM_176795.3:c.183_439dup (HRAS)
XM_011519875.1:c.-424-5128_-424-4719dup (LRRC56)	XP_011518177.1:n.-424-5128_-424-4719dup
XM_011519877.1:c.-162+5133_-162+5542dup (LRRC56)	XP_011518179.1:n.-162+5133_-162+5542dup
XR_242795.1:n.382_638dup (HRAS)
NM_001130442.2:c.183_439dup (HRAS)
NM_001318054.1:c.-137_120dup (HRAS)
NM_005343.3:c.183_439dup (HRAS)
NM_176795.4:c.183_439dup (HRAS)
XM_011519875.2:c.-424-5128_-424-4719dup (LRRC56)	XP_011518177.1:n.-424-5128_-424-4719dup
XM_011519877.2:c.-162+5133_-162+5542dup (LRRC56)	XP_011518179.1:n.-162+5133_-162+5542dup
XM_017017167.1:c.-499-5053_-499-4644dup (LRRC56)	XP_016872656.1:n.-499-5053_-499-4644dup
XM_017017168.1:c.-499-5053_-499-4644dup (LRRC56)	XP_016872657.1:n.-499-5053_-499-4644dup
NM_005343.4:c.183_439dup (HRAS)
NM_001318054.2:c.-137_120dup (HRAS)
NM_001130442.3:c.183_439dup (HRAS)
NM_176795.5:c.183_439dup (HRAS)