Canonical Allele Identifier: CA2790128360

Gene: HRAS LRRC56

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.534191_534213del , CM000673.2:g.534191_534213del	GRCh38
NC_000011.9:g.534191_534213del , CM000673.1:g.534191_534213del	GRCh37
NC_000011.8:g.524191_524213del	NCBI36
NG_007666.1:g.6343_6365del

Transcript Alleles

HGVS	Amino-acid change
ENST00000397594.7:c.111+4_111+26del (HRAS)
ENST00000417302.7:c.111+4_111+26del (HRAS)
ENST00000417302.6:c.111+4_111+26del (HRAS)
ENST00000462734.2:c.111+4_111+26del (HRAS)
ENST00000311189.8:c.111+4_111+26del (HRAS)
ENST00000311189.7:c.111+4_111+26del (HRAS)
ENST00000397594.5:c.111+4_111+26del (HRAS)
ENST00000397596.6:c.111+4_111+26del (HRAS)
ENST00000417302.5:c.111+4_111+26del (HRAS)
ENST00000451590.5:c.111+4_111+26del (HRAS)
ENST00000468682.2:n.599+4_599+26del (HRAS)
ENST00000493230.5:c.111+4_111+26del (HRAS)
NM_001130442.1:c.111+4_111+26del (HRAS)
NM_005343.2:c.111+4_111+26del (HRAS)
NM_176795.3:c.111+4_111+26del (HRAS)
XM_011519875.1:c.-424-4407_-424-4385del (LRRC56)	XP_011518177.1:n.-424-4407_-424-4385del
XM_011519877.1:c.-161-5389_-161-5367del (LRRC56)	XP_011518179.1:n.-161-5389_-161-5367del
XR_242795.1:n.310+4_310+26del (HRAS)
NM_001130442.2:c.111+4_111+26del (HRAS)
NM_001318054.1:c.-209+4_-209+26del (HRAS)
NM_005343.3:c.111+4_111+26del (HRAS)
NM_176795.4:c.111+4_111+26del (HRAS)
XM_011519875.2:c.-424-4407_-424-4385del (LRRC56)	XP_011518177.1:n.-424-4407_-424-4385del
XM_011519877.2:c.-161-5389_-161-5367del (LRRC56)	XP_011518179.1:n.-161-5389_-161-5367del
XM_017017167.1:c.-499-4332_-499-4310del (LRRC56)	XP_016872656.1:n.-499-4332_-499-4310del
XM_017017168.1:c.-499-4332_-499-4310del (LRRC56)	XP_016872657.1:n.-499-4332_-499-4310del
NM_005343.4:c.111+4_111+26del (HRAS)
NM_001318054.2:c.-209+4_-209+26del (HRAS)
NM_001130442.3:c.111+4_111+26del (HRAS)
NM_176795.5:c.111+4_111+26del (HRAS)