Canonical Allele Identifier: CA378921066

Gene: HRAS LRRC56

Linked Data

• ClinVar Variation Id: 462156
• ClinVar RCV Id: RCV000526328 ; RCV001260727
• dbSNP Id: rs1171786943
• gnomAD v4: 11-532688-G-A
• MyVariant Identifiers: chr11:g.532688G>A (hg19) ; chr11:g.532688G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.532688G>A , CM000673.2:g.532688G>A	GRCh38
NC_000011.9:g.532688G>A , CM000673.1:g.532688G>A	GRCh37
NC_000011.8:g.522688G>A	NCBI36
NG_007666.1:g.7863C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397594.7:c.*20-58C>T (HRAS)	ENSP00000380722.3:n.*20-58C>T
ENST00000417302.7:c.*87C>T (HRAS) MANE Plus Clinical	ENSP00000388246.1:n.*87C>T
ENST00000397594.6:c.251-58C>T (HRAS)	ENSP00000380722.2:n.251-58C>T
ENST00000417302.6:c.*87C>T (HRAS)	ENSP00000388246.1:n.*87C>T
ENST00000462734.2:c.*130C>T (HRAS)	ENSP00000507303.1:n.*130C>T
ENST00000311189.8:c.518C>T (HRAS) MANE Select	ENSP00000309845.7:p.Pro173Leu
ENST00000311189.7:c.518C>T (HRAS)	ENSP00000309845.7:p.Pro173Leu
ENST00000397594.5:c.*87C>T (HRAS)	ENSP00000380722.1:n.*87C>T
ENST00000397596.6:c.518C>T (HRAS)	ENSP00000380723.2:p.Pro173Leu
ENST00000417302.5:c.*87C>T (HRAS)	ENSP00000388246.1:n.*87C>T
ENST00000451590.5:c.518C>T (HRAS)	ENSP00000407586.1:p.Pro173Leu
ENST00000462734.1:n.293C>T (HRAS)
ENST00000478324.5:n.243-58C>T (HRAS)
ENST00000479482.1:n.439C>T (HRAS)
ENST00000493230.5:c.*87C>T (HRAS)	ENSP00000434023.1:n.*87C>T
NM_001130442.1:c.518C>T (HRAS)	NP_001123914.1:p.Pro173Leu
NM_005343.2:c.518C>T (HRAS)	NP_005334.1:p.Pro173Leu
NM_176795.3:c.*87C>T (HRAS)	NP_789765.1:n.*87C>T
XM_011519875.1:c.-425+4351G>A (LRRC56)	XP_011518177.1:n.-425+4351G>A
XM_011519877.1:c.-162+4351G>A (LRRC56)	XP_011518179.1:n.-162+4351G>A
XR_242795.1:n.799C>T (HRAS)
NM_001130442.2:c.518C>T (HRAS)	NP_001123914.1:p.Pro173Leu
NM_001318054.1:c.281C>T (HRAS)	NP_001304983.1:p.Pro94Leu
NM_005343.3:c.518C>T (HRAS)	NP_005334.1:p.Pro173Leu
NM_176795.4:c.*87C>T (HRAS)	NP_789765.1:n.*87C>T
XM_011519875.2:c.-425+4351G>A (LRRC56)	XP_011518177.1:n.-425+4351G>A
XM_011519877.2:c.-162+4351G>A (LRRC56)	XP_011518179.1:n.-162+4351G>A
XM_017017167.1:c.-500+4351G>A (LRRC56)	XP_016872656.1:n.-500+4351G>A
XM_017017168.1:c.-500+4351G>A (LRRC56)	XP_016872657.1:n.-500+4351G>A
NM_005343.4:c.518C>T (HRAS) MANE Select	NP_005334.1:p.Pro173Leu
NM_001318054.2:c.281C>T (HRAS)	NP_001304983.1:p.Pro94Leu
NM_001130442.3:c.518C>T (HRAS)	NP_001123914.1:p.Pro173Leu
NM_176795.5:c.*87C>T (HRAS) MANE Plus Clinical	NP_789765.1:n.*87C>T