Canonical Allele Identifier: CA2658715274

Gene: SOS1

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39014854G>T , CM000664.2:g.39014854G>T	GRCh38
NC_000002.11:g.39241995G>T , CM000664.1:g.39241995G>T	GRCh37
NC_000002.10:g.39095499G>T	NCBI36
NG_007530.1:g.110610C>A , LRG_754:g.110610C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685279.1:c.626-8C>A	ENSP00000509424.1:n.626-8C>A
ENST00000688043.1:n.2080-8C>A
ENST00000689668.1:n.1866-8C>A
ENST00000690876.1:c.1748-8C>A	ENSP00000508955.1:n.1748-8C>A
ENST00000691229.1:c.1748-8C>A	ENSP00000510437.1:n.1748-8C>A
ENST00000692089.1:c.1748-8C>A	ENSP00000508626.1:n.1748-8C>A
ENST00000692620.1:c.626-8C>A	ENSP00000509311.1:n.626-8C>A
ENST00000402219.8:c.1859-8C>A MANE Select	ENSP00000384675.2:n.1859-8C>A
ENST00000395038.6:c.1859-8C>A	ENSP00000378479.2:n.1859-8C>A
ENST00000402219.6:c.1859-8C>A	ENSP00000384675.2:n.1859-8C>A
ENST00000426016.5:c.1859-8C>A	ENSP00000387784.1:n.1859-8C>A
NM_005633.3:c.1859-8C>A , LRG_754t1:c.1859-8C>A	NP_005624.2:n.1859-8C>A
XM_005264515.3:c.1859-8C>A	XP_005264572.1:n.1859-8C>A
XM_011533060.1:c.1952-8C>A	XP_011531362.1:n.1952-8C>A
XM_011533061.1:c.1952-8C>A	XP_011531363.1:n.1952-8C>A
XM_011533062.1:c.1838-8C>A	XP_011531364.1:n.1838-8C>A
XM_011533063.1:c.1835-8C>A	XP_011531365.1:n.1835-8C>A
XM_011533064.1:c.1688-8C>A	XP_011531366.1:n.1688-8C>A
XM_011533065.1:c.1952-8C>A	XP_011531367.1:n.1952-8C>A
XM_011533066.1:c.794-8C>A	XP_011531368.1:n.794-8C>A
XM_005264515.4:c.1859-8C>A	XP_005264572.1:n.1859-8C>A
XM_011533062.2:c.1838-8C>A	XP_011531364.1:n.1838-8C>A
XM_011533064.2:c.1688-8C>A	XP_011531366.1:n.1688-8C>A
NM_001382394.1:c.1838-8C>A	NP_001369323.1:n.1838-8C>A
NM_001382395.1:c.1859-8C>A	NP_001369324.1:n.1859-8C>A
NM_005633.4:c.1859-8C>A MANE Select	NP_005624.2:n.1859-8C>A