Canonical Allele Identifier: CA7177490

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50188612T>C , CM000676.2:g.50188612T>C	GRCh38
NC_000014.8:g.50655330T>C , CM000676.1:g.50655330T>C	GRCh37
NC_000014.7:g.49725080T>C	NCBI36
NG_051073.1:g.48082A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006939.4:c.599A>G MANE Select	NP_008870.2:p.Tyr200Cys
ENST00000216373.10:c.599A>G MANE Select	ENSP00000216373.5:p.Tyr200Cys
NM_006939.2:c.599A>G	NP_008870.2:p.Tyr200Cys
NM_006939.3:c.599A>G	NP_008870.2:p.Tyr200Cys
ENST00000216373.9:c.599A>G	ENSP00000216373.5:p.Tyr200Cys
ENST00000543680.5:c.599A>G	ENSP00000445328.1:p.Tyr200Cys
ENST00000556469.5:n.482-6006A>G
XM_005268021.1:c.419A>G	XP_005268078.1:p.Tyr140Cys
XM_011537103.1:c.560A>G	XP_011535405.1:p.Tyr187Cys
XM_011537104.1:c.599A>G	XP_011535406.1:p.Tyr200Cys
XR_943842.1:n.1039+4740T>C
XR_943843.1:n.1039+4740T>C