Canonical Allele Identifier: CA486173180

Gene: SOS2

Linked Data

• MyVariant Identifiers: chr14:g.50666505T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50199787T>A , CM000676.2:g.50199787T>A	GRCh38
NC_000014.8:g.50666505T>A , CM000676.1:g.50666505T>A	GRCh37
NC_000014.7:g.49736255T>A	NCBI36
NG_051073.1:g.36907A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.414A>T MANE Select	ENSP00000216373.5:p.Ser138=
ENST00000216373.9:c.414A>T	ENSP00000216373.5:p.Ser138=
ENST00000543680.5:c.414A>T	ENSP00000445328.1:p.Ser138=
ENST00000555666.1:n.593A>T
ENST00000556469.5:n.385A>T
NM_006939.2:c.414A>T	NP_008870.2:p.Ser138=
XM_005268021.1:c.234A>T	XP_005268078.1:p.Ser78=
XM_011537103.1:c.375A>T	XP_011535405.1:p.Ser125=
XM_011537104.1:c.414A>T	XP_011535406.1:p.Ser138=
XR_943842.1:n.1039+15915T>A
XR_943843.1:n.1039+15915T>A
NM_006939.3:c.414A>T	NP_008870.2:p.Ser138=
NM_006939.4:c.414A>T MANE Select	NP_008870.2:p.Ser138=