Canonical Allele Identifier: CA1624197
Gene: SOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38989267_38989270del , CM000664.2:g.38989267_38989270del GRCh38
NC_000002.11:g.39216408_39216411del , CM000664.1:g.39216408_39216411del GRCh37
NC_000002.10:g.39069912_39069915del NCBI36
NG_007530.1:g.136197_136200del , LRG_754:g.136197_136200del

Transcript Alleles

HGVS Amino-acid Change
ENST00000685279.1:c.2158+3_2158+6del
ENST00000686849.1:n.182+3_182+6del
ENST00000690876.1:c.*697+3_*697+6del
ENST00000692089.1:c.3280+3_3280+6del
ENST00000692227.1:c.1043-1676_1043-1673del ENSP00000509138.1:n.1043-1676_1043-1673del
ENST00000402219.8:c.3391+3_3391+6del
ENST00000395038.6:c.3347-1676_3347-1673del ENSP00000378479.2:n.3347-1676_3347-1673del
ENST00000402219.6:c.3391+3_3391+6del
ENST00000426016.5:c.3391+3_3391+6del
NM_005633.3:c.3391+3_3391+6del , LRG_754t1:c.3391+3_3391+6del
XM_005264515.3:c.3347-1676_3347-1673del XP_005264572.1:n.3347-1676_3347-1673del
XM_011533060.1:c.3484+3_3484+6del
XM_011533061.1:c.3440-1676_3440-1673del XP_011531363.1:n.3440-1676_3440-1673del
XM_011533062.1:c.3370+3_3370+6del
XM_011533063.1:c.3367+3_3367+6del
XM_011533064.1:c.3220+3_3220+6del
XM_011533065.1:c.3484+3_3484+6del
XM_011533066.1:c.2326+3_2326+6del
XM_005264515.4:c.3347-1676_3347-1673del XP_005264572.1:n.3347-1676_3347-1673del
XM_011533062.2:c.3370+3_3370+6del
XM_011533064.2:c.3220+3_3220+6del
NM_001382394.1:c.3370+3_3370+6del
NM_001382395.1:c.3347-1676_3347-1673del NP_001369324.1:n.3347-1676_3347-1673del
NM_005633.4:c.3391+3_3391+6del