Canonical Allele Identifier: CA2136066050

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50153053_50153054delinsAC , CM000676.2:g.50153053_50153054delinsAC	GRCh38
NC_000014.8:g.50619771_50619772delinsAC , CM000676.1:g.50619771_50619772delinsAC	GRCh37
NC_000014.7:g.49689521_49689522delinsAC	NCBI36
NG_051073.1:g.83640_83641delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.2161+16_2161+17delinsGT MANE Select	ENSP00000216373.5:n.2161+16_2161+17delinsGT
ENST00000216373.9:c.2161+16_2161+17delinsGT	ENSP00000216373.5:n.2161+16_2161+17delinsGT
ENST00000543680.5:c.2062+16_2062+17delinsGT	ENSP00000445328.1:n.2062+16_2062+17delinsGT
NM_006939.2:c.2161+16_2161+17delinsGT	NP_008870.2:n.2161+16_2161+17delinsGT
XM_005268021.1:c.1981+16_1981+17delinsGT	XP_005268078.1:n.1981+16_1981+17delinsGT
XM_011537103.1:c.2122+16_2122+17delinsGT	XP_011535405.1:n.2122+16_2122+17delinsGT
XM_011537104.1:c.2161+16_2161+17delinsGT	XP_011535406.1:n.2161+16_2161+17delinsGT
NM_006939.3:c.2161+16_2161+17delinsGT	NP_008870.2:n.2161+16_2161+17delinsGT
NM_006939.4:c.2161+16_2161+17delinsGT MANE Select	NP_008870.2:n.2161+16_2161+17delinsGT