Canonical Allele Identifier: CA2624771082
Gene: SOS2 HGNC NCBI

Linked Data

gnomAD v4: 14-50150265-ACTTG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50150266_50150269del , CM000676.2:g.50150266_50150269del GRCh38
NC_000014.8:g.50616984_50616987del , CM000676.1:g.50616984_50616987del GRCh37
NC_000014.7:g.49686734_49686737del NCBI36
NG_051073.1:g.86425_86428del

Transcript Alleles

HGVS Amino-acid change
ENST00000216373.10:c.2162-39_2162-36del MANE Select ENSP00000216373.5:n.2162-39_2162-36del
ENST00000216373.9:c.2162-39_2162-36del ENSP00000216373.5:n.2162-39_2162-36del
ENST00000543680.5:c.2063-39_2063-36del ENSP00000445328.1:n.2063-39_2063-36del
NM_006939.2:c.2162-39_2162-36del NP_008870.2:n.2162-39_2162-36del
XM_005268021.1:c.1982-39_1982-36del XP_005268078.1:n.1982-39_1982-36del
XM_011537103.1:c.2123-39_2123-36del XP_011535405.1:n.2123-39_2123-36del
XM_011537104.1:c.2162-39_2162-36del XP_011535406.1:n.2162-39_2162-36del
NM_006939.3:c.2162-39_2162-36del NP_008870.2:n.2162-39_2162-36del
NM_006939.4:c.2162-39_2162-36del MANE Select NP_008870.2:n.2162-39_2162-36del
Search 100 bp 5'
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