Canonical Allele Identifier: CA2739276055

Gene: HRAS LRRC56

Linked Data

• ClinVar Variation Id: 2853311
• ClinVar RCV Id: RCV003628571

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.533440_533466del , CM000673.2:g.533440_533466del	GRCh38
NC_000011.9:g.533440_533466del , CM000673.1:g.533440_533466del	GRCh37
NC_000011.8:g.523440_523466del	NCBI36
NG_007666.1:g.7088_7114del

Transcript Alleles

HGVS	Amino-acid change
ENST00000397594.7:c.440_450+16del (HRAS)
ENST00000417302.7:c.440_450+16del (HRAS)
ENST00000397594.6:c.158_168+16del (HRAS)
ENST00000417302.6:c.440_450+16del (HRAS)
ENST00000462734.2:c.440_450+16del (HRAS)
ENST00000311189.8:c.440_450+16del (HRAS)
ENST00000311189.7:c.440_450+16del (HRAS)
ENST00000397594.5:c.440_450+16del (HRAS)
ENST00000397596.6:c.440_450+16del (HRAS)
ENST00000417302.5:c.440_450+16del (HRAS)
ENST00000451590.5:c.440_450+16del (HRAS)
ENST00000462734.1:n.133_143+16del (HRAS)
ENST00000478324.5:n.150_160+16del (HRAS)
ENST00000479482.1:n.361_371+16del (HRAS)
ENST00000493230.5:c.440_450+16del (HRAS)
NM_001130442.1:c.440_450+16del (HRAS)
NM_005343.2:c.440_450+16del (HRAS)
NM_176795.3:c.440_450+16del (HRAS)
XM_011519875.1:c.-425+5103_-425+5129del (LRRC56)	XP_011518177.1:n.-425+5103_-425+5129del
XM_011519877.1:c.-162+5103_-162+5129del (LRRC56)	XP_011518179.1:n.-162+5103_-162+5129del
XR_242795.1:n.639_649+16del (HRAS)
NM_001130442.2:c.440_450+16del (HRAS)
NM_001318054.1:c.121_131+16del (HRAS)
NM_005343.3:c.440_450+16del (HRAS)
NM_176795.4:c.440_450+16del (HRAS)
XM_011519875.2:c.-425+5103_-425+5129del (LRRC56)	XP_011518177.1:n.-425+5103_-425+5129del
XM_011519877.2:c.-162+5103_-162+5129del (LRRC56)	XP_011518179.1:n.-162+5103_-162+5129del
XM_017017167.1:c.-499-5083_-499-5057del (LRRC56)	XP_016872656.1:n.-499-5083_-499-5057del
XM_017017168.1:c.-499-5083_-499-5057del (LRRC56)	XP_016872657.1:n.-499-5083_-499-5057del
NM_005343.4:c.440_450+16del (HRAS)
NM_001318054.2:c.121_131+16del (HRAS)
NM_001130442.3:c.440_450+16del (HRAS)
NM_176795.5:c.440_450+16del (HRAS)