Canonical Allele Identifier: CA389645007

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50159511T>G , CM000676.2:g.50159511T>G	GRCh38
NC_000014.8:g.50626229T>G , CM000676.1:g.50626229T>G	GRCh37
NC_000014.7:g.49695979T>G	NCBI36
NG_051073.1:g.77183A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_006939.4:c.1772A>C MANE Select	NP_008870.2:p.Gln591Pro
ENST00000216373.10:c.1772A>C MANE Select	ENSP00000216373.5:p.Gln591Pro
NM_006939.2:c.1772A>C	NP_008870.2:p.Gln591Pro
NM_006939.3:c.1772A>C	NP_008870.2:p.Gln591Pro
ENST00000216373.9:c.1772A>C	ENSP00000216373.5:p.Gln591Pro
ENST00000543680.5:c.1673A>C	ENSP00000445328.1:p.Gln558Pro
ENST00000555794.2:c.886A>C
XM_005268021.1:c.1592A>C	XP_005268078.1:p.Gln531Pro
XM_011537103.1:c.1733A>C	XP_011535405.1:p.Gln578Pro
XM_011537104.1:c.1772A>C	XP_011535406.1:p.Gln591Pro