Canonical Allele Identifier: CA2658715358

Gene: SOS1

Linked Data

• gnomAD v4: 2-39022376-TAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39022383_39022384del , CM000664.2:g.39022383_39022384del	GRCh38
NC_000002.11:g.39249524_39249525del , CM000664.1:g.39249524_39249525del	GRCh37
NC_000002.10:g.39103028_39103029del	NCBI36
NG_007530.1:g.103086_103087del , LRG_754:g.103086_103087del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000472480.2:n.1930_1931del
ENST00000685279.1:c.625+192_625+193del	ENSP00000509424.1:n.625+192_625+193del
ENST00000688043.1:n.2079+192_2079+193del
ENST00000689668.1:n.1865+192_1865+193del
ENST00000690876.1:c.1747+192_1747+193del	ENSP00000508955.1:n.1747+192_1747+193del
ENST00000691229.1:c.1747+192_1747+193del	ENSP00000510437.1:n.1747+192_1747+193del
ENST00000692089.1:c.1747+192_1747+193del	ENSP00000508626.1:n.1747+192_1747+193del
ENST00000692620.1:c.625+192_625+193del	ENSP00000509311.1:n.625+192_625+193del
ENST00000402219.8:c.1858+192_1858+193del MANE Select	ENSP00000384675.2:n.1858+192_1858+193del
ENST00000395038.6:c.1858+192_1858+193del	ENSP00000378479.2:n.1858+192_1858+193del
ENST00000402219.6:c.1858+192_1858+193del	ENSP00000384675.2:n.1858+192_1858+193del
ENST00000426016.5:c.1858+192_1858+193del	ENSP00000387784.1:n.1858+192_1858+193del
NM_005633.3:c.1858+192_1858+193del , LRG_754t1:c.1858+192_1858+193del	NP_005624.2:n.1858+192_1858+193del
XM_005264515.3:c.1858+192_1858+193del	XP_005264572.1:n.1858+192_1858+193del
XM_011533060.1:c.1951+192_1951+193del	XP_011531362.1:n.1951+192_1951+193del
XM_011533061.1:c.1951+192_1951+193del	XP_011531363.1:n.1951+192_1951+193del
XM_011533062.1:c.1837+192_1837+193del	XP_011531364.1:n.1837+192_1837+193del
XM_011533063.1:c.1834+192_1834+193del	XP_011531365.1:n.1834+192_1834+193del
XM_011533064.1:c.1687+192_1687+193del	XP_011531366.1:n.1687+192_1687+193del
XM_011533065.1:c.1951+192_1951+193del	XP_011531367.1:n.1951+192_1951+193del
XM_011533066.1:c.793+192_793+193del	XP_011531368.1:n.793+192_793+193del
XM_005264515.4:c.1858+192_1858+193del	XP_005264572.1:n.1858+192_1858+193del
XM_011533062.2:c.1837+192_1837+193del	XP_011531364.1:n.1837+192_1837+193del
XM_011533064.2:c.1687+192_1687+193del	XP_011531366.1:n.1687+192_1687+193del
NM_001382394.1:c.1837+192_1837+193del	NP_001369323.1:n.1837+192_1837+193del
NM_001382395.1:c.1858+192_1858+193del	NP_001369324.1:n.1858+192_1858+193del
NM_005633.4:c.1858+192_1858+193del MANE Select	NP_005624.2:n.1858+192_1858+193del