Canonical Allele Identifier: CA2573147051

Gene: HRAS LRRC56

Linked Data

• ClinVar Variation Id: 1677298
• ClinVar RCV Id: RCV002223165
• dbSNP Id: rs2133985401

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.533358_533370del , CM000673.2:g.533358_533370del	GRCh38
NC_000011.9:g.533358_533370del , CM000673.1:g.533358_533370del	GRCh37
NC_000011.8:g.523358_523370del	NCBI36
NG_007666.1:g.7181_7193del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397594.7:c.451-12_451del (HRAS)
ENST00000417302.7:c.451-12_451del (HRAS)
ENST00000397594.6:c.169-12_169del (HRAS)
ENST00000417302.6:c.451-12_451del (HRAS)
ENST00000462734.2:c.451-17_451-5del (HRAS)	ENSP00000507303.1:n.451-17_451-5del
ENST00000311189.8:c.450+83_450+95del (HRAS) MANE Select	ENSP00000309845.7:n.450+83_450+95del
ENST00000311189.7:c.450+83_450+95del (HRAS)	ENSP00000309845.7:n.450+83_450+95del
ENST00000397594.5:c.451-12_451del (HRAS)
ENST00000397596.6:c.450+83_450+95del (HRAS)	ENSP00000380723.2:n.450+83_450+95del
ENST00000417302.5:c.451-12_451del (HRAS)
ENST00000451590.5:c.450+83_450+95del (HRAS)	ENSP00000407586.1:n.450+83_450+95del
ENST00000462734.1:n.144-12_144del (HRAS)
ENST00000478324.5:n.161-12_161del (HRAS)
ENST00000479482.1:n.371+83_371+95del (HRAS)
ENST00000493230.5:c.451-12_451del (HRAS)
NM_001130442.1:c.450+83_450+95del (HRAS)	NP_001123914.1:n.450+83_450+95del
NM_005343.2:c.450+83_450+95del (HRAS)	NP_005334.1:n.450+83_450+95del
NM_176795.3:c.451-12_451del (HRAS)
XM_011519875.1:c.-425+5021_-425+5033del (LRRC56)	XP_011518177.1:n.-425+5021_-425+5033del
XM_011519877.1:c.-162+5021_-162+5033del (LRRC56)	XP_011518179.1:n.-162+5021_-162+5033del
XR_242795.1:n.650-12_650del (HRAS)
NM_001130442.2:c.450+83_450+95del (HRAS)	NP_001123914.1:n.450+83_450+95del
NM_001318054.1:c.132-12_132del (HRAS)
NM_005343.3:c.450+83_450+95del (HRAS)	NP_005334.1:n.450+83_450+95del
NM_176795.4:c.451-12_451del (HRAS)
XM_011519875.2:c.-425+5021_-425+5033del (LRRC56)	XP_011518177.1:n.-425+5021_-425+5033del
XM_011519877.2:c.-162+5021_-162+5033del (LRRC56)	XP_011518179.1:n.-162+5021_-162+5033del
XM_017017167.1:c.-500+5021_-500+5033del (LRRC56)	XP_016872656.1:n.-500+5021_-500+5033del
XM_017017168.1:c.-500+5021_-500+5033del (LRRC56)	XP_016872657.1:n.-500+5021_-500+5033del
NM_005343.4:c.450+83_450+95del (HRAS) MANE Select	NP_005334.1:n.450+83_450+95del
NM_001318054.2:c.132-12_132del (HRAS)
NM_001130442.3:c.450+83_450+95del (HRAS)	NP_001123914.1:n.450+83_450+95del
NM_176795.5:c.451-12_451del (HRAS)