Canonical Allele Identifier: CA2658715470

Gene: SOS1

Linked Data

• gnomAD v4: 2-39022553-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39022553A>G , CM000664.2:g.39022553A>G	GRCh38
NC_000002.11:g.39249694A>G , CM000664.1:g.39249694A>G	GRCh37
NC_000002.10:g.39103198A>G	NCBI36
NG_007530.1:g.102911T>C , LRG_754:g.102911T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000472480.2:n.1755T>C
ENST00000685279.1:c.625+17T>C	ENSP00000509424.1:n.625+17T>C
ENST00000688043.1:n.2079+17T>C
ENST00000689668.1:n.1865+17T>C
ENST00000690876.1:c.1747+17T>C	ENSP00000508955.1:n.1747+17T>C
ENST00000691229.1:c.1747+17T>C	ENSP00000510437.1:n.1747+17T>C
ENST00000692089.1:c.1747+17T>C	ENSP00000508626.1:n.1747+17T>C
ENST00000692620.1:c.625+17T>C	ENSP00000509311.1:n.625+17T>C
ENST00000402219.8:c.1858+17T>C MANE Select	ENSP00000384675.2:n.1858+17T>C
ENST00000395038.6:c.1858+17T>C	ENSP00000378479.2:n.1858+17T>C
ENST00000402219.6:c.1858+17T>C	ENSP00000384675.2:n.1858+17T>C
ENST00000426016.5:c.1858+17T>C	ENSP00000387784.1:n.1858+17T>C
NM_005633.3:c.1858+17T>C , LRG_754t1:c.1858+17T>C	NP_005624.2:n.1858+17T>C
XM_005264515.3:c.1858+17T>C	XP_005264572.1:n.1858+17T>C
XM_011533060.1:c.1951+17T>C	XP_011531362.1:n.1951+17T>C
XM_011533061.1:c.1951+17T>C	XP_011531363.1:n.1951+17T>C
XM_011533062.1:c.1837+17T>C	XP_011531364.1:n.1837+17T>C
XM_011533063.1:c.1834+17T>C	XP_011531365.1:n.1834+17T>C
XM_011533064.1:c.1687+17T>C	XP_011531366.1:n.1687+17T>C
XM_011533065.1:c.1951+17T>C	XP_011531367.1:n.1951+17T>C
XM_011533066.1:c.793+17T>C	XP_011531368.1:n.793+17T>C
XM_005264515.4:c.1858+17T>C	XP_005264572.1:n.1858+17T>C
XM_011533062.2:c.1837+17T>C	XP_011531364.1:n.1837+17T>C
XM_011533064.2:c.1687+17T>C	XP_011531366.1:n.1687+17T>C
NM_001382394.1:c.1837+17T>C	NP_001369323.1:n.1837+17T>C
NM_001382395.1:c.1858+17T>C	NP_001369324.1:n.1858+17T>C
NM_005633.4:c.1858+17T>C MANE Select	NP_005624.2:n.1858+17T>C