Canonical Allele Identifier: CA7177611

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50204414A>T , CM000676.2:g.50204414A>T	GRCh38
NC_000014.8:g.50671132A>T , CM000676.1:g.50671132A>T	GRCh37
NC_000014.7:g.49740882A>T	NCBI36
NG_051073.1:g.32280T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006939.4:c.88-5T>A MANE Select	NP_008870.2:n.88-5T>A
ENST00000216373.10:c.88-5T>A MANE Select	ENSP00000216373.5:n.88-5T>A
NM_006939.2:c.88-5T>A	NP_008870.2:n.88-5T>A
NM_006939.3:c.88-5T>A	NP_008870.2:n.88-5T>A
ENST00000216373.9:c.88-5T>A	ENSP00000216373.5:n.88-5T>A
ENST00000543680.5:c.88-5T>A	ENSP00000445328.1:n.88-5T>A
ENST00000555666.1:n.267-5T>A
ENST00000556452.1:c.147-5T>A	ENSP00000452553.1:n.147-5T>A
ENST00000556469.5:n.59-5T>A
XM_005268021.1:c.-93-5T>A	XP_005268078.1:n.-93-5T>A
XM_011537103.1:c.49-5T>A	XP_011535405.1:n.49-5T>A
XM_011537104.1:c.88-5T>A	XP_011535406.1:n.88-5T>A
XR_943842.1:n.1039+20542A>T
XR_943843.1:n.1039+20542A>T