Canonical Allele Identifier: CA2611691513
Gene: HRAS HGNC NCBI
LRRC56 HGNC NCBI

Linked Data

gnomAD v4: 11-532430-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532430C>A , CM000673.2:g.532430C>A GRCh38
NC_000011.9:g.532430C>A , CM000673.1:g.532430C>A GRCh37
NC_000011.8:g.522430C>A NCBI36
NG_007666.1:g.8121G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*220G>T (HRAS) ENSP00000380722.3:n.*220G>T
ENST00000417302.7:c.*345G>T (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*345G>T
ENST00000397594.6:c.451G>T (HRAS) ENSP00000380722.2:n.451G>T
ENST00000417302.6:c.*345G>T (HRAS) ENSP00000388246.1:n.*345G>T
ENST00000462734.2:c.*280G>T (HRAS) ENSP00000507303.1:n.*280G>T
ENST00000311189.8:c.*98G>T (HRAS) MANE Select ENSP00000309845.7:n.*98G>T
ENST00000311189.7:c.*98G>T (HRAS) ENSP00000309845.7:n.*98G>T
ENST00000397594.5:c.*345G>T (HRAS) ENSP00000380722.1:n.*345G>T
ENST00000397596.6:c.*206G>T (HRAS) ENSP00000380723.2:n.*206G>T
ENST00000417302.5:c.*345G>T (HRAS) ENSP00000388246.1:n.*345G>T
ENST00000451590.5:c.*206G>T (HRAS) ENSP00000407586.1:n.*206G>T
ENST00000462734.1:n.443G>T (HRAS)
ENST00000478324.5:n.443G>T (HRAS)
ENST00000493230.5:c.*237G>T (HRAS) ENSP00000434023.1:n.*237G>T
NM_001130442.1:c.*206G>T (HRAS) NP_001123914.1:n.*206G>T
NM_005343.2:c.*98G>T (HRAS) NP_005334.1:n.*98G>T
NM_176795.3:c.*345G>T (HRAS) NP_789765.1:n.*345G>T
XM_011519875.1:c.-425+4093C>A (LRRC56) XP_011518177.1:n.-425+4093C>A
XM_011519877.1:c.-162+4093C>A (LRRC56) XP_011518179.1:n.-162+4093C>A
XR_242795.1:n.949G>T (HRAS)
NM_001130442.2:c.*206G>T (HRAS) NP_001123914.1:n.*206G>T
NM_001318054.1:c.*98G>T (HRAS) NP_001304983.1:n.*98G>T
NM_005343.3:c.*98G>T (HRAS) NP_005334.1:n.*98G>T
NM_176795.4:c.*345G>T (HRAS) NP_789765.1:n.*345G>T
XM_011519875.2:c.-425+4093C>A (LRRC56) XP_011518177.1:n.-425+4093C>A
XM_011519877.2:c.-162+4093C>A (LRRC56) XP_011518179.1:n.-162+4093C>A
XM_017017167.1:c.-500+4093C>A (LRRC56) XP_016872656.1:n.-500+4093C>A
XM_017017168.1:c.-500+4093C>A (LRRC56) XP_016872657.1:n.-500+4093C>A
NM_005343.4:c.*98G>T (HRAS) MANE Select NP_005334.1:n.*98G>T
NM_001318054.2:c.*98G>T (HRAS) NP_001304983.1:n.*98G>T
NM_001130442.3:c.*206G>T (HRAS) NP_001123914.1:n.*206G>T
NM_176795.5:c.*345G>T (HRAS) MANE Plus Clinical NP_789765.1:n.*345G>T
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