Canonical Allele Identifier: CA346365396

Gene: SOS1

Linked Data

• MyVariant Identifiers: chr2:g.39249789G>A (hg19) ; chr2:g.39022648G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39022648G>A , CM000664.2:g.39022648G>A	GRCh38
NC_000002.11:g.39249789G>A , CM000664.1:g.39249789G>A	GRCh37
NC_000002.10:g.39103293G>A	NCBI36
NG_007530.1:g.102816C>T , LRG_754:g.102816C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000472480.2:n.1660C>T
ENST00000685279.1:c.547C>T	ENSP00000509424.1:p.Pro183Ser
ENST00000688043.1:n.2001C>T
ENST00000689668.1:n.1787C>T
ENST00000690876.1:c.1669C>T	ENSP00000508955.1:p.Pro557Ser
ENST00000691229.1:c.1669C>T	ENSP00000510437.1:p.Pro557Ser
ENST00000692089.1:c.1669C>T	ENSP00000508626.1:p.Pro557Ser
ENST00000692620.1:c.547C>T	ENSP00000509311.1:p.Pro183Ser
ENST00000402219.8:c.1780C>T MANE Select	ENSP00000384675.2:p.Pro594Ser
ENST00000395038.6:c.1780C>T	ENSP00000378479.2:p.Pro594Ser
ENST00000402219.6:c.1780C>T	ENSP00000384675.2:p.Pro594Ser
ENST00000426016.5:c.1780C>T	ENSP00000387784.1:p.Pro594Ser
NM_005633.3:c.1780C>T , LRG_754t1:c.1780C>T	NP_005624.2:p.Pro594Ser
XM_005264515.3:c.1780C>T	XP_005264572.1:p.Pro594Ser
XM_011533060.1:c.1873C>T	XP_011531362.1:p.Pro625Ser
XM_011533061.1:c.1873C>T	XP_011531363.1:p.Pro625Ser
XM_011533062.1:c.1759C>T	XP_011531364.1:p.Pro587Ser
XM_011533063.1:c.1756C>T	XP_011531365.1:p.Pro586Ser
XM_011533064.1:c.1609C>T	XP_011531366.1:p.Pro537Ser
XM_011533065.1:c.1873C>T	XP_011531367.1:p.Pro625Ser
XM_011533066.1:c.715C>T	XP_011531368.1:p.Pro239Ser
XM_005264515.4:c.1780C>T	XP_005264572.1:p.Pro594Ser
XM_011533062.2:c.1759C>T	XP_011531364.1:p.Pro587Ser
XM_011533064.2:c.1609C>T	XP_011531366.1:p.Pro537Ser
NM_001382394.1:c.1759C>T	NP_001369323.1:p.Pro587Ser
NM_001382395.1:c.1780C>T	NP_001369324.1:p.Pro594Ser
NM_005633.4:c.1780C>T MANE Select	NP_005624.2:p.Pro594Ser