Canonical Allele Identifier: CA2801534799

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180721_50180722del , CM000676.2:g.50180721_50180722del	GRCh38
NC_000014.8:g.50647439_50647440del , CM000676.1:g.50647439_50647440del	GRCh37
NC_000014.7:g.49717189_49717190del	NCBI36
NG_051073.1:g.55973_55974del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.859-39_859-38del MANE Select	ENSP00000216373.5:n.859-39_859-38del
ENST00000216373.9:c.859-39_859-38del	ENSP00000216373.5:n.859-39_859-38del
ENST00000543680.5:c.859-39_859-38del	ENSP00000445328.1:n.859-39_859-38del
NM_006939.2:c.859-39_859-38del	NP_008870.2:n.859-39_859-38del
XM_005268021.1:c.679-39_679-38del	XP_005268078.1:n.679-39_679-38del
XM_011537103.1:c.820-39_820-38del	XP_011535405.1:n.820-39_820-38del
XM_011537104.1:c.859-39_859-38del	XP_011535406.1:n.859-39_859-38del
XR_943842.1:n.954-3066_954-3065del
XR_943843.1:n.954-3066_954-3065del
NM_006939.3:c.859-39_859-38del	NP_008870.2:n.859-39_859-38del
NM_006939.4:c.859-39_859-38del MANE Select	NP_008870.2:n.859-39_859-38del