Canonical Allele Identifier: CA1246140193

Gene: SOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39023244_39023250delinsCATTATT , CM000664.2:g.39023244_39023250delinsCATTATT	GRCh38
NC_000002.11:g.39250385_39250391delinsCATTATT , CM000664.1:g.39250385_39250391delinsCATTATT	GRCh37
NC_000002.10:g.39103889_39103895delinsCATTATT	NCBI36
NG_007530.1:g.102214_102220delinsAATAATG , LRG_754:g.102214_102220delinsAATAATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000472480.2:n.1083-25_1083-19delinsAATAATG
ENST00000685279.1:c.-31-25_-31-19delinsAATAATG	ENSP00000509424.1:n.-31-25_-31-19delinsAATAATG
ENST00000688043.1:n.1424-25_1424-19delinsAATAATG
ENST00000689668.1:n.1210-25_1210-19delinsAATAATG
ENST00000690679.1:c.1390-25_1390-19delinsAATAATG
ENST00000690876.1:c.1092-25_1092-19delinsAATAATG	ENSP00000508955.1:n.1092-25_1092-19delinsAATAATG
ENST00000691229.1:c.1092-25_1092-19delinsAATAATG	ENSP00000510437.1:n.1092-25_1092-19delinsAATAATG
ENST00000692089.1:c.1092-25_1092-19delinsAATAATG	ENSP00000508626.1:n.1092-25_1092-19delinsAATAATG
ENST00000692620.1:c.-31-25_-31-19delinsAATAATG	ENSP00000509311.1:n.-31-25_-31-19delinsAATAATG
ENST00000402219.8:c.1203-25_1203-19delinsAATAATG MANE Select	ENSP00000384675.2:n.1203-25_1203-19delinsAATAATG
ENST00000395038.6:c.1203-25_1203-19delinsAATAATG	ENSP00000378479.2:n.1203-25_1203-19delinsAATAATG
ENST00000402219.6:c.1203-25_1203-19delinsAATAATG	ENSP00000384675.2:n.1203-25_1203-19delinsAATAATG
ENST00000426016.5:c.1203-25_1203-19delinsAATAATG	ENSP00000387784.1:n.1203-25_1203-19delinsAATAATG
ENST00000472480.1:n.47-25_47-19delinsAATAATG
NM_005633.3:c.1203-25_1203-19delinsAATAATG , LRG_754t1:c.1203-25_1203-19delinsAATAATG	NP_005624.2:n.1203-25_1203-19delinsAATAATG
XM_005264515.3:c.1203-25_1203-19delinsAATAATG	XP_005264572.1:n.1203-25_1203-19delinsAATAATG
XM_011533060.1:c.1296-25_1296-19delinsAATAATG	XP_011531362.1:n.1296-25_1296-19delinsAATAATG
XM_011533061.1:c.1296-25_1296-19delinsAATAATG	XP_011531363.1:n.1296-25_1296-19delinsAATAATG
XM_011533062.1:c.1182-25_1182-19delinsAATAATG	XP_011531364.1:n.1182-25_1182-19delinsAATAATG
XM_011533063.1:c.1179-25_1179-19delinsAATAATG	XP_011531365.1:n.1179-25_1179-19delinsAATAATG
XM_011533064.1:c.1032-25_1032-19delinsAATAATG	XP_011531366.1:n.1032-25_1032-19delinsAATAATG
XM_011533065.1:c.1296-25_1296-19delinsAATAATG	XP_011531367.1:n.1296-25_1296-19delinsAATAATG
XM_011533066.1:c.138-25_138-19delinsAATAATG	XP_011531368.1:n.138-25_138-19delinsAATAATG
XM_005264515.4:c.1203-25_1203-19delinsAATAATG	XP_005264572.1:n.1203-25_1203-19delinsAATAATG
XM_011533062.2:c.1182-25_1182-19delinsAATAATG	XP_011531364.1:n.1182-25_1182-19delinsAATAATG
XM_011533064.2:c.1032-25_1032-19delinsAATAATG	XP_011531366.1:n.1032-25_1032-19delinsAATAATG
NM_001382394.1:c.1182-25_1182-19delinsAATAATG	NP_001369323.1:n.1182-25_1182-19delinsAATAATG
NM_001382395.1:c.1203-25_1203-19delinsAATAATG	NP_001369324.1:n.1203-25_1203-19delinsAATAATG
NM_005633.4:c.1203-25_1203-19delinsAATAATG MANE Select	NP_005624.2:n.1203-25_1203-19delinsAATAATG