Canonical Allele Identifier: CA346364455

Gene: SOS1

Linked Data

• MyVariant Identifiers: chr2:g.39239476T>A (hg19) ; chr2:g.39012335T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39012335T>A , CM000664.2:g.39012335T>A	GRCh38
NC_000002.11:g.39239476T>A , CM000664.1:g.39239476T>A	GRCh37
NC_000002.10:g.39092980T>A	NCBI36
NG_007530.1:g.113129A>T , LRG_754:g.113129A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685279.1:c.948A>T	ENSP00000509424.1:p.Lys316Asn
ENST00000688043.1:n.3513A>T
ENST00000689668.1:n.2188A>T
ENST00000690514.1:n.270A>T
ENST00000690876.1:c.2070A>T	ENSP00000508955.1:p.Lys690Asn
ENST00000691229.1:c.2070A>T	ENSP00000510437.1:p.Lys690Asn
ENST00000692089.1:c.2070A>T	ENSP00000508626.1:p.Lys690Asn
ENST00000692620.1:c.934+1125A>T	ENSP00000509311.1:n.934+1125A>T
ENST00000402219.8:c.2181A>T MANE Select	ENSP00000384675.2:p.Lys727Asn
ENST00000395038.6:c.2181A>T	ENSP00000378479.2:p.Lys727Asn
ENST00000402219.6:c.2181A>T	ENSP00000384675.2:p.Lys727Asn
ENST00000426016.5:c.2181A>T	ENSP00000387784.1:p.Lys727Asn
NM_005633.3:c.2181A>T , LRG_754t1:c.2181A>T	NP_005624.2:p.Lys727Asn
XM_005264515.3:c.2181A>T	XP_005264572.1:p.Lys727Asn
XM_011533060.1:c.2274A>T	XP_011531362.1:p.Lys758Asn
XM_011533061.1:c.2274A>T	XP_011531363.1:p.Lys758Asn
XM_011533062.1:c.2160A>T	XP_011531364.1:p.Lys720Asn
XM_011533063.1:c.2157A>T	XP_011531365.1:p.Lys719Asn
XM_011533064.1:c.2010A>T	XP_011531366.1:p.Lys670Asn
XM_011533065.1:c.2274A>T	XP_011531367.1:p.Lys758Asn
XM_011533066.1:c.1116A>T	XP_011531368.1:p.Lys372Asn
XM_005264515.4:c.2181A>T	XP_005264572.1:p.Lys727Asn
XM_011533062.2:c.2160A>T	XP_011531364.1:p.Lys720Asn
XM_011533064.2:c.2010A>T	XP_011531366.1:p.Lys670Asn
NM_001382394.1:c.2160A>T	NP_001369323.1:p.Lys720Asn
NM_001382395.1:c.2181A>T	NP_001369324.1:p.Lys727Asn
NM_005633.4:c.2181A>T MANE Select	NP_005624.2:p.Lys727Asn