Canonical Allele Identifier: CA2624771217
Gene: SOS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50152955dup , CM000676.2:g.50152955dup GRCh38
NC_000014.8:g.50619673dup , CM000676.1:g.50619673dup GRCh37
NC_000014.7:g.49689423dup NCBI36
NG_051073.1:g.83739dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000216373.10:c.2161+115dup MANE Select ENSP00000216373.5:n.2161+115dup
ENST00000216373.9:c.2161+115dup ENSP00000216373.5:n.2161+115dup
ENST00000543680.5:c.2062+115dup ENSP00000445328.1:n.2062+115dup
NM_006939.2:c.2161+115dup NP_008870.2:n.2161+115dup
XM_005268021.1:c.1981+115dup XP_005268078.1:n.1981+115dup
XM_011537103.1:c.2122+115dup XP_011535405.1:n.2122+115dup
XM_011537104.1:c.2161+115dup XP_011535406.1:n.2161+115dup
NM_006939.3:c.2161+115dup NP_008870.2:n.2161+115dup
NM_006939.4:c.2161+115dup MANE Select NP_008870.2:n.2161+115dup