Canonical Allele Identifier: CA378922560

Gene: HRAS LRRC56

Linked Data

• dbSNP Id: rs1212027549
• MyVariant Identifiers: chr11:g.533354C>G (hg19) ; chr11:g.533354C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.533354C>G , CM000673.2:g.533354C>G	GRCh38
NC_000011.9:g.533354C>G , CM000673.1:g.533354C>G	GRCh37
NC_000011.8:g.523354C>G	NCBI36
NG_007666.1:g.7197G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000397594.7:c.455G>C (HRAS)	ENSP00000380722.3:p.Ser152Thr
ENST00000417302.7:c.455G>C (HRAS) MANE Plus Clinical	ENSP00000388246.1:p.Ser152Thr
ENST00000397594.6:c.173G>C (HRAS)	ENSP00000380722.2:p.Ser58Thr
ENST00000417302.6:c.455G>C (HRAS)	ENSP00000388246.1:p.Ser152Thr
ENST00000462734.2:c.451-1G>C (HRAS)	ENSP00000507303.1:n.451-1G>C
ENST00000311189.8:c.450+99G>C (HRAS) MANE Select	ENSP00000309845.7:n.450+99G>C
ENST00000311189.7:c.450+99G>C (HRAS)	ENSP00000309845.7:n.450+99G>C
ENST00000397594.5:c.455G>C (HRAS)	ENSP00000380722.1:p.Ser152Thr
ENST00000397596.6:c.450+99G>C (HRAS)	ENSP00000380723.2:n.450+99G>C
ENST00000417302.5:c.455G>C (HRAS)	ENSP00000388246.1:p.Ser152Thr
ENST00000451590.5:c.450+99G>C (HRAS)	ENSP00000407586.1:n.450+99G>C
ENST00000462734.1:n.148G>C (HRAS)
ENST00000478324.5:n.165G>C (HRAS)
ENST00000479482.1:n.371+99G>C (HRAS)
ENST00000493230.5:c.455G>C (HRAS)	ENSP00000434023.1:p.Ser152Thr
NM_001130442.1:c.450+99G>C (HRAS)	NP_001123914.1:n.450+99G>C
NM_005343.2:c.450+99G>C (HRAS)	NP_005334.1:n.450+99G>C
NM_176795.3:c.455G>C (HRAS)	NP_789765.1:p.Ser152Thr
XM_011519875.1:c.-425+5017C>G (LRRC56)	XP_011518177.1:n.-425+5017C>G
XM_011519877.1:c.-162+5017C>G (LRRC56)	XP_011518179.1:n.-162+5017C>G
XR_242795.1:n.654G>C (HRAS)
NM_001130442.2:c.450+99G>C (HRAS)	NP_001123914.1:n.450+99G>C
NM_001318054.1:c.136G>C (HRAS)	NP_001304983.1:p.Ala46Pro
NM_005343.3:c.450+99G>C (HRAS)	NP_005334.1:n.450+99G>C
NM_176795.4:c.455G>C (HRAS)	NP_789765.1:p.Ser152Thr
XM_011519875.2:c.-425+5017C>G (LRRC56)	XP_011518177.1:n.-425+5017C>G
XM_011519877.2:c.-162+5017C>G (LRRC56)	XP_011518179.1:n.-162+5017C>G
XM_017017167.1:c.-500+5017C>G (LRRC56)	XP_016872656.1:n.-500+5017C>G
XM_017017168.1:c.-500+5017C>G (LRRC56)	XP_016872657.1:n.-500+5017C>G
NM_005343.4:c.450+99G>C (HRAS) MANE Select	NP_005334.1:n.450+99G>C
NM_001318054.2:c.136G>C (HRAS)	NP_001304983.1:p.Ala46Pro
NM_001130442.3:c.450+99G>C (HRAS)	NP_001123914.1:n.450+99G>C
NM_176795.5:c.455G>C (HRAS) MANE Plus Clinical	NP_789765.1:p.Ser152Thr