Canonical Allele Identifier: CA2658715835

Gene: SOS1

Linked Data

• gnomAD v4: 2-39024006-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39024006T>C , CM000664.2:g.39024006T>C	GRCh38
NC_000002.11:g.39251147T>C , CM000664.1:g.39251147T>C	GRCh37
NC_000002.10:g.39104651T>C	NCBI36
NG_007530.1:g.101458A>G , LRG_754:g.101458A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000472480.2:n.1082+4A>G
ENST00000688043.1:n.1423+4A>G
ENST00000689668.1:n.1209+4A>G
ENST00000690679.1:c.1389+4A>G
ENST00000690876.1:c.1091+4A>G	ENSP00000508955.1:n.1091+4A>G
ENST00000691229.1:c.1091+4A>G	ENSP00000510437.1:n.1091+4A>G
ENST00000692089.1:c.1091+4A>G	ENSP00000508626.1:n.1091+4A>G
ENST00000402219.8:c.1202+4A>G MANE Select	ENSP00000384675.2:n.1202+4A>G
ENST00000395038.6:c.1202+4A>G	ENSP00000378479.2:n.1202+4A>G
ENST00000402219.6:c.1202+4A>G	ENSP00000384675.2:n.1202+4A>G
ENST00000426016.5:c.1202+4A>G	ENSP00000387784.1:n.1202+4A>G
NM_005633.3:c.1202+4A>G , LRG_754t1:c.1202+4A>G	NP_005624.2:n.1202+4A>G
XM_005264515.3:c.1202+4A>G	XP_005264572.1:n.1202+4A>G
XM_011533060.1:c.1295+4A>G	XP_011531362.1:n.1295+4A>G
XM_011533061.1:c.1295+4A>G	XP_011531363.1:n.1295+4A>G
XM_011533062.1:c.1181+4A>G	XP_011531364.1:n.1181+4A>G
XM_011533063.1:c.1178+4A>G	XP_011531365.1:n.1178+4A>G
XM_011533064.1:c.1031+4A>G	XP_011531366.1:n.1031+4A>G
XM_011533065.1:c.1295+4A>G	XP_011531367.1:n.1295+4A>G
XM_011533066.1:c.137+4A>G	XP_011531368.1:n.137+4A>G
XM_005264515.4:c.1202+4A>G	XP_005264572.1:n.1202+4A>G
XM_011533062.2:c.1181+4A>G	XP_011531364.1:n.1181+4A>G
XM_011533064.2:c.1031+4A>G	XP_011531366.1:n.1031+4A>G
NM_001382394.1:c.1181+4A>G	NP_001369323.1:n.1181+4A>G
NM_001382395.1:c.1202+4A>G	NP_001369324.1:n.1202+4A>G
NM_005633.4:c.1202+4A>G MANE Select	NP_005624.2:n.1202+4A>G