Canonical Allele Identifier: CA389640339

Gene: SOS2

Linked Data

• MyVariant Identifiers: chr14:g.50597225A>T (hg19) ; chr14:g.50130507A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50130507A>T , CM000676.2:g.50130507A>T	GRCh38
NC_000014.8:g.50597225A>T , CM000676.1:g.50597225A>T	GRCh37
NC_000014.7:g.49666975A>T	NCBI36
NG_051073.1:g.106187T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000216373.10:c.3331T>A MANE Select	ENSP00000216373.5:p.Ser1111Thr
ENST00000216373.9:c.3331T>A	ENSP00000216373.5:p.Ser1111Thr
ENST00000543680.5:c.3232T>A	ENSP00000445328.1:p.Ser1078Thr
NM_006939.2:c.3331T>A	NP_008870.2:p.Ser1111Thr
XM_005268021.1:c.3151T>A	XP_005268078.1:p.Ser1051Thr
XM_011537103.1:c.3292T>A	XP_011535405.1:p.Ser1098Thr
NM_006939.3:c.3331T>A	NP_008870.2:p.Ser1111Thr
NM_006939.4:c.3331T>A MANE Select	NP_008870.2:p.Ser1111Thr