Canonical Allele Identifier: CA472322563

Gene: HRAS LRRC56

Linked Data

• MyVariant Identifiers: chr11:g.534305C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.534305C>A , CM000673.2:g.534305C>A	GRCh38
NC_000011.9:g.534305C>A , CM000673.1:g.534305C>A	GRCh37
NC_000011.8:g.524305C>A	NCBI36
NG_007666.1:g.6246G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397594.7:c.18G>T (HRAS)	ENSP00000380722.3:p.Leu6=
ENST00000417302.7:c.18G>T (HRAS) MANE Plus Clinical	ENSP00000388246.1:p.Leu6=
ENST00000417302.6:c.18G>T (HRAS)	ENSP00000388246.1:p.Leu6=
ENST00000462734.2:c.18G>T (HRAS)	ENSP00000507303.1:p.Leu6=
ENST00000311189.8:c.18G>T (HRAS) MANE Select	ENSP00000309845.7:p.Leu6=
ENST00000311189.7:c.18G>T (HRAS)	ENSP00000309845.7:p.Leu6=
ENST00000397594.5:c.18G>T (HRAS)	ENSP00000380722.1:p.Leu6=
ENST00000397596.6:c.18G>T (HRAS)	ENSP00000380723.2:p.Leu6=
ENST00000417302.5:c.18G>T (HRAS)	ENSP00000388246.1:p.Leu6=
ENST00000451590.5:c.18G>T (HRAS)	ENSP00000407586.1:p.Leu6=
ENST00000468682.2:n.506G>T (HRAS)
ENST00000482021.1:n.141G>T (HRAS)
ENST00000493230.5:c.18G>T (HRAS)	ENSP00000434023.1:p.Leu6=
NM_001130442.1:c.18G>T (HRAS)	NP_001123914.1:p.Leu6=
NM_005343.2:c.18G>T (HRAS)	NP_005334.1:p.Leu6=
NM_176795.3:c.18G>T (HRAS)	NP_789765.1:p.Leu6=
XM_011519875.1:c.-424-4293C>A (LRRC56)	XP_011518177.1:n.-424-4293C>A
XM_011519877.1:c.-161-5275C>A (LRRC56)	XP_011518179.1:n.-161-5275C>A
XR_242795.1:n.217G>T (HRAS)
NM_001130442.2:c.18G>T (HRAS)	NP_001123914.1:p.Leu6=
NM_001318054.1:c.-302G>T (HRAS)	NP_001304983.1:n.-302G>T
NM_005343.3:c.18G>T (HRAS)	NP_005334.1:p.Leu6=
NM_176795.4:c.18G>T (HRAS)	NP_789765.1:p.Leu6=
XM_011519875.2:c.-424-4293C>A (LRRC56)	XP_011518177.1:n.-424-4293C>A
XM_011519877.2:c.-161-5275C>A (LRRC56)	XP_011518179.1:n.-161-5275C>A
XM_017017167.1:c.-499-4218C>A (LRRC56)	XP_016872656.1:n.-499-4218C>A
XM_017017168.1:c.-499-4218C>A (LRRC56)	XP_016872657.1:n.-499-4218C>A
NM_005343.4:c.18G>T (HRAS) MANE Select	NP_005334.1:p.Leu6=
NM_001318054.2:c.-302G>T (HRAS)	NP_001304983.1:n.-302G>T
NM_001130442.3:c.18G>T (HRAS)	NP_001123914.1:p.Leu6=
NM_176795.5:c.18G>T (HRAS) MANE Plus Clinical	NP_789765.1:p.Leu6=