Canonical Allele Identifier: CA2136039818
Gene: SOS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50150260_50150262delinsCTT , CM000676.2:g.50150260_50150262delinsCTT GRCh38
NC_000014.8:g.50616978_50616980delinsCTT , CM000676.1:g.50616978_50616980delinsCTT GRCh37
NC_000014.7:g.49686728_49686730delinsCTT NCBI36
NG_051073.1:g.86432_86434delinsAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000216373.10:c.2162-32_2162-30delinsAAG MANE Select ENSP00000216373.5:n.2162-32_2162-30delins...
ENST00000216373.9:c.2162-32_2162-30delinsAAG ENSP00000216373.5:n.2162-32_2162-30delins...
ENST00000543680.5:c.2063-32_2063-30delinsAAG ENSP00000445328.1:n.2063-32_2063-30delins...
NM_006939.2:c.2162-32_2162-30delinsAAG NP_008870.2:n.2162-32_2162-30delinsAAG
XM_005268021.1:c.1982-32_1982-30delinsAAG XP_005268078.1:n.1982-32_1982-30delinsAAG...
XM_011537103.1:c.2123-32_2123-30delinsAAG XP_011535405.1:n.2123-32_2123-30delinsAAG...
XM_011537104.1:c.2162-32_2162-30delinsAAG XP_011535406.1:n.2162-32_2162-30delinsAAG...
NM_006939.3:c.2162-32_2162-30delinsAAG NP_008870.2:n.2162-32_2162-30delinsAAG
NM_006939.4:c.2162-32_2162-30delinsAAG MANE Select NP_008870.2:n.2162-32_2162-30delinsAAG
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