Canonical Allele Identifier: CA389647952

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50188508A>G , CM000676.2:g.50188508A>G	GRCh38
NC_000014.8:g.50655226A>G , CM000676.1:g.50655226A>G	GRCh37
NC_000014.7:g.49724976A>G	NCBI36
NG_051073.1:g.48186T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_006939.4:c.703T>C MANE Select	NP_008870.2:p.Phe235Leu
ENST00000216373.10:c.703T>C MANE Select	ENSP00000216373.5:p.Phe235Leu
NM_006939.2:c.703T>C	NP_008870.2:p.Phe235Leu
NM_006939.3:c.703T>C	NP_008870.2:p.Phe235Leu
ENST00000216373.9:c.703T>C	ENSP00000216373.5:p.Phe235Leu
ENST00000543680.5:c.703T>C	ENSP00000445328.1:p.Phe235Leu
ENST00000556469.5:n.482-5902T>C
XM_005268021.1:c.523T>C	XP_005268078.1:p.Phe175Leu
XM_011537103.1:c.664T>C	XP_011535405.1:p.Phe222Leu
XM_011537104.1:c.703T>C	XP_011535406.1:p.Phe235Leu
XR_943842.1:n.1039+4636A>G
XR_943843.1:n.1039+4636A>G