Canonical Allele Identifier: CA2573147048

Gene: HRAS LRRC56

Linked Data

• dbSNP Id: rs2133982475

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.532731_532732del , CM000673.2:g.532731_532732del	GRCh38
NC_000011.9:g.532731_532732del , CM000673.1:g.532731_532732del	GRCh37
NC_000011.8:g.522731_522732del	NCBI36
NG_007666.1:g.7819_7820del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397594.7:c.*20-102_*20-101del (HRAS)	ENSP00000380722.3:n.*20-102_*20-101del
ENST00000417302.7:c.*43_*44del (HRAS) MANE Plus Clinical	ENSP00000388246.1:n.*43_*44del
ENST00000397594.6:c.251-102_251-101del (HRAS)	ENSP00000380722.2:n.251-102_251-101del
ENST00000417302.6:c.*43_*44del (HRAS)	ENSP00000388246.1:n.*43_*44del
ENST00000462734.2:c.*86_*87del (HRAS)	ENSP00000507303.1:n.*86_*87del
ENST00000311189.8:c.474_475del (HRAS) MANE Select	ENSP00000309845.7:p.Leu159GlyfsTer3
ENST00000311189.7:c.474_475del (HRAS)	ENSP00000309845.7:p.Leu159GlyfsTer3
ENST00000397594.5:c.*43_*44del (HRAS)	ENSP00000380722.1:n.*43_*44del
ENST00000397596.6:c.474_475del (HRAS)	ENSP00000380723.2:p.Leu159GlyfsTer3
ENST00000417302.5:c.*43_*44del (HRAS)	ENSP00000388246.1:n.*43_*44del
ENST00000451590.5:c.474_475del (HRAS)	ENSP00000407586.1:p.Leu159GlyfsTer3
ENST00000462734.1:n.249_250del (HRAS)
ENST00000478324.5:n.243-102_243-101del (HRAS)
ENST00000479482.1:n.395_396del (HRAS)
ENST00000493230.5:c.*43_*44del (HRAS)	ENSP00000434023.1:n.*43_*44del
NM_001130442.1:c.474_475del (HRAS)	NP_001123914.1:p.Leu159GlyfsTer3
NM_005343.2:c.474_475del (HRAS)	NP_005334.1:p.Leu159GlyfsTer3
NM_176795.3:c.*43_*44del (HRAS)	NP_789765.1:n.*43_*44del
XM_011519875.1:c.-425+4394_-425+4395del (LRRC56)	XP_011518177.1:n.-425+4394_-425+4395del
XM_011519877.1:c.-162+4394_-162+4395del (LRRC56)	XP_011518179.1:n.-162+4394_-162+4395del
XR_242795.1:n.755_756del (HRAS)
NM_001130442.2:c.474_475del (HRAS)	NP_001123914.1:p.Leu159GlyfsTer3
NM_001318054.1:c.237_238del (HRAS)	NP_001304983.1:p.Leu80GlyfsTer3
NM_005343.3:c.474_475del (HRAS)	NP_005334.1:p.Leu159GlyfsTer3
NM_176795.4:c.*43_*44del (HRAS)	NP_789765.1:n.*43_*44del
XM_011519875.2:c.-425+4394_-425+4395del (LRRC56)	XP_011518177.1:n.-425+4394_-425+4395del
XM_011519877.2:c.-162+4394_-162+4395del (LRRC56)	XP_011518179.1:n.-162+4394_-162+4395del
XM_017017167.1:c.-500+4394_-500+4395del (LRRC56)	XP_016872656.1:n.-500+4394_-500+4395del
XM_017017168.1:c.-500+4394_-500+4395del (LRRC56)	XP_016872657.1:n.-500+4394_-500+4395del
NM_005343.4:c.474_475del (HRAS) MANE Select	NP_005334.1:p.Leu159GlyfsTer3
NM_001318054.2:c.237_238del (HRAS)	NP_001304983.1:p.Leu80GlyfsTer3
NM_001130442.3:c.474_475del (HRAS)	NP_001123914.1:p.Leu159GlyfsTer3
NM_176795.5:c.*43_*44del (HRAS) MANE Plus Clinical	NP_789765.1:n.*43_*44del