Canonical Allele Identifier: CA1246153656

Gene: SOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39054565_39054566delinsCA , CM000664.2:g.39054565_39054566delinsCA	GRCh38
NC_000002.11:g.39281706_39281707delinsCA , CM000664.1:g.39281706_39281707delinsCA	GRCh37
NC_000002.10:g.39135210_39135211delinsCA	NCBI36
NG_007530.1:g.70898_70899delinsTG , LRG_754:g.70898_70899delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461545.2:n.747+48_747+49delinsTG
ENST00000685782.1:n.1558+48_1558+49delinsTG
ENST00000688189.1:n.533_534delinsTG
ENST00000689668.1:n.727+48_727+49delinsTG
ENST00000690679.1:c.820+48_820+49delinsTG
ENST00000690876.1:c.720+48_720+49delinsTG	ENSP00000508955.1:n.720+48_720+49delinsTG
ENST00000691229.1:c.720+48_720+49delinsTG	ENSP00000510437.1:n.720+48_720+49delinsTG
ENST00000692089.1:c.720+48_720+49delinsTG	ENSP00000508626.1:n.720+48_720+49delinsTG
ENST00000402219.8:c.720+48_720+49delinsTG MANE Select	ENSP00000384675.2:n.720+48_720+49delinsTG
ENST00000395038.6:c.720+48_720+49delinsTG	ENSP00000378479.2:n.720+48_720+49delinsTG
ENST00000402219.6:c.720+48_720+49delinsTG	ENSP00000384675.2:n.720+48_720+49delinsTG
ENST00000426016.5:c.720+48_720+49delinsTG	ENSP00000387784.1:n.720+48_720+49delinsTG
NM_005633.3:c.720+48_720+49delinsTG , LRG_754t1:c.720+48_720+49delinsTG	NP_005624.2:n.720+48_720+49delinsTG
XM_005264515.3:c.720+48_720+49delinsTG	XP_005264572.1:n.720+48_720+49delinsTG
XM_011533060.1:c.813+48_813+49delinsTG	XP_011531362.1:n.813+48_813+49delinsTG
XM_011533061.1:c.813+48_813+49delinsTG	XP_011531363.1:n.813+48_813+49delinsTG
XM_011533062.1:c.699+48_699+49delinsTG	XP_011531364.1:n.699+48_699+49delinsTG
XM_011533063.1:c.696+48_696+49delinsTG	XP_011531365.1:n.696+48_696+49delinsTG
XM_011533064.1:c.549+48_549+49delinsTG	XP_011531366.1:n.549+48_549+49delinsTG
XM_011533065.1:c.813+48_813+49delinsTG	XP_011531367.1:n.813+48_813+49delinsTG
XM_005264515.4:c.720+48_720+49delinsTG	XP_005264572.1:n.720+48_720+49delinsTG
XM_011533062.2:c.699+48_699+49delinsTG	XP_011531364.1:n.699+48_699+49delinsTG
XM_011533064.2:c.549+48_549+49delinsTG	XP_011531366.1:n.549+48_549+49delinsTG
NM_001382394.1:c.699+48_699+49delinsTG	NP_001369323.1:n.699+48_699+49delinsTG
NM_001382395.1:c.720+48_720+49delinsTG	NP_001369324.1:n.720+48_720+49delinsTG
NM_005633.4:c.720+48_720+49delinsTG MANE Select	NP_005624.2:n.720+48_720+49delinsTG