Canonical Allele Identifier: CA7177606

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50204376T>C , CM000676.2:g.50204376T>C	GRCh38
NC_000014.8:g.50671094T>C , CM000676.1:g.50671094T>C	GRCh37
NC_000014.7:g.49740844T>C	NCBI36
NG_051073.1:g.32318A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006939.4:c.121A>G MANE Select	NP_008870.2:p.Asn41Asp
ENST00000216373.10:c.121A>G MANE Select	ENSP00000216373.5:p.Asn41Asp
NM_006939.2:c.121A>G	NP_008870.2:p.Asn41Asp
NM_006939.3:c.121A>G	NP_008870.2:p.Asn41Asp
ENST00000216373.9:c.121A>G	ENSP00000216373.5:p.Asn41Asp
ENST00000543680.5:c.121A>G	ENSP00000445328.1:p.Asn41Asp
ENST00000555666.1:n.300A>G
ENST00000556452.1:c.180A>G	ENSP00000452553.1:p.Leu60=
ENST00000556469.5:n.92A>G
XM_005268021.1:c.-60A>G	XP_005268078.1:n.-60A>G
XM_011537103.1:c.82A>G	XP_011535405.1:p.Asn28Asp
XM_011537104.1:c.121A>G	XP_011535406.1:p.Asn41Asp
XR_943842.1:n.1039+20504T>C
XR_943843.1:n.1039+20504T>C