Canonical Allele Identifier: CA389649646

Gene: SOS2

Linked Data

• MyVariant Identifiers: chr14:g.50666503G>A (hg19) ; chr14:g.50199785G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50199785G>A , CM000676.2:g.50199785G>A	GRCh38
NC_000014.8:g.50666503G>A , CM000676.1:g.50666503G>A	GRCh37
NC_000014.7:g.49736253G>A	NCBI36
NG_051073.1:g.36909C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.416C>T MANE Select	ENSP00000216373.5:p.Ala139Val
ENST00000216373.9:c.416C>T	ENSP00000216373.5:p.Ala139Val
ENST00000543680.5:c.416C>T	ENSP00000445328.1:p.Ala139Val
ENST00000555666.1:n.595C>T
ENST00000556469.5:n.387C>T
NM_006939.2:c.416C>T	NP_008870.2:p.Ala139Val
XM_005268021.1:c.236C>T	XP_005268078.1:p.Ala79Val
XM_011537103.1:c.377C>T	XP_011535405.1:p.Ala126Val
XM_011537104.1:c.416C>T	XP_011535406.1:p.Ala139Val
XR_943842.1:n.1039+15913G>A
XR_943843.1:n.1039+15913G>A
NM_006939.3:c.416C>T	NP_008870.2:p.Ala139Val
NM_006939.4:c.416C>T MANE Select	NP_008870.2:p.Ala139Val