Canonical Allele Identifier: CA10615202

Gene: SOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38982258_38982260del , CM000664.2:g.38982258_38982260del	GRCh38
NC_000002.11:g.39209399_39209401del , CM000664.1:g.39209399_39209401del	GRCh37
NC_000002.10:g.39062903_39062905del	NCBI36
NG_007530.1:g.143206_143208del , LRG_754:g.143206_143208del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685279.1:c.*3566_*3568del	ENSP00000509424.1:n.*3566_*3568del
ENST00000692089.1:c.3399+5215_3399+5217del	ENSP00000508626.1:n.3399+5215_3399+5217del
ENST00000402219.8:c.*3566_*3568del MANE Select	ENSP00000384675.2:n.*3566_*3568del
ENST00000402219.6:c.*3566_*3568del	ENSP00000384675.2:n.*3566_*3568del
ENST00000426016.5:c.*3566_*3568del	ENSP00000387784.1:n.*3566_*3568del
NM_005633.3:c.*3566_*3568del , LRG_754t1:c.*3566_*3568del	NP_005624.2:n.*3566_*3568del
XM_005264515.3:c.*3566_*3568del	XP_005264572.1:n.*3566_*3568del
XM_011533060.1:c.*3566_*3568del	XP_011531362.1:n.*3566_*3568del
XM_011533061.1:c.*3566_*3568del	XP_011531363.1:n.*3566_*3568del
XM_011533062.1:c.*3566_*3568del	XP_011531364.1:n.*3566_*3568del
XM_011533063.1:c.*3566_*3568del	XP_011531365.1:n.*3566_*3568del
XM_011533064.1:c.*3566_*3568del	XP_011531366.1:n.*3566_*3568del
XM_011533065.1:c.*3052_*3054del	XP_011531367.1:n.*3052_*3054del
XM_011533066.1:c.*3566_*3568del	XP_011531368.1:n.*3566_*3568del
NM_001382394.1:c.*3566_*3568del	NP_001369323.1:n.*3566_*3568del
NM_001382395.1:c.*3566_*3568del	NP_001369324.1:n.*3566_*3568del
NM_005633.4:c.*3566_*3568del MANE Select	NP_005624.2:n.*3566_*3568del