Canonical Allele Identifier: CA2611690673

Gene: HRAS LRRC56

Linked Data

• gnomAD v4: 11-533366-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.533366A>C , CM000673.2:g.533366A>C	GRCh38
NC_000011.9:g.533366A>C , CM000673.1:g.533366A>C	GRCh37
NC_000011.8:g.523366A>C	NCBI36
NG_007666.1:g.7185T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397594.7:c.451-8T>G (HRAS)	ENSP00000380722.3:n.451-8T>G
ENST00000417302.7:c.451-8T>G (HRAS) MANE Plus Clinical	ENSP00000388246.1:n.451-8T>G
ENST00000397594.6:c.169-8T>G (HRAS)	ENSP00000380722.2:n.169-8T>G
ENST00000417302.6:c.451-8T>G (HRAS)	ENSP00000388246.1:n.451-8T>G
ENST00000462734.2:c.451-13T>G (HRAS)	ENSP00000507303.1:n.451-13T>G
ENST00000311189.8:c.450+87T>G (HRAS) MANE Select	ENSP00000309845.7:n.450+87T>G
ENST00000311189.7:c.450+87T>G (HRAS)	ENSP00000309845.7:n.450+87T>G
ENST00000397594.5:c.451-8T>G (HRAS)	ENSP00000380722.1:n.451-8T>G
ENST00000397596.6:c.450+87T>G (HRAS)	ENSP00000380723.2:n.450+87T>G
ENST00000417302.5:c.451-8T>G (HRAS)	ENSP00000388246.1:n.451-8T>G
ENST00000451590.5:c.450+87T>G (HRAS)	ENSP00000407586.1:n.450+87T>G
ENST00000462734.1:n.144-8T>G (HRAS)
ENST00000478324.5:n.161-8T>G (HRAS)
ENST00000479482.1:n.371+87T>G (HRAS)
ENST00000493230.5:c.451-8T>G (HRAS)	ENSP00000434023.1:n.451-8T>G
NM_001130442.1:c.450+87T>G (HRAS)	NP_001123914.1:n.450+87T>G
NM_005343.2:c.450+87T>G (HRAS)	NP_005334.1:n.450+87T>G
NM_176795.3:c.451-8T>G (HRAS)	NP_789765.1:n.451-8T>G
XM_011519875.1:c.-425+5029A>C (LRRC56)	XP_011518177.1:n.-425+5029A>C
XM_011519877.1:c.-162+5029A>C (LRRC56)	XP_011518179.1:n.-162+5029A>C
XR_242795.1:n.650-8T>G (HRAS)
NM_001130442.2:c.450+87T>G (HRAS)	NP_001123914.1:n.450+87T>G
NM_001318054.1:c.132-8T>G (HRAS)	NP_001304983.1:n.132-8T>G
NM_005343.3:c.450+87T>G (HRAS)	NP_005334.1:n.450+87T>G
NM_176795.4:c.451-8T>G (HRAS)	NP_789765.1:n.451-8T>G
XM_011519875.2:c.-425+5029A>C (LRRC56)	XP_011518177.1:n.-425+5029A>C
XM_011519877.2:c.-162+5029A>C (LRRC56)	XP_011518179.1:n.-162+5029A>C
XM_017017167.1:c.-500+5029A>C (LRRC56)	XP_016872656.1:n.-500+5029A>C
XM_017017168.1:c.-500+5029A>C (LRRC56)	XP_016872657.1:n.-500+5029A>C
NM_005343.4:c.450+87T>G (HRAS) MANE Select	NP_005334.1:n.450+87T>G
NM_001318054.2:c.132-8T>G (HRAS)	NP_001304983.1:n.132-8T>G
NM_001130442.3:c.450+87T>G (HRAS)	NP_001123914.1:n.450+87T>G
NM_176795.5:c.451-8T>G (HRAS) MANE Plus Clinical	NP_789765.1:n.451-8T>G