Canonical Allele Identifier: CA389647115

Gene: SOS2

Linked Data

• MyVariant Identifiers: chr14:g.50647387T>A (hg19) ; chr14:g.50180669T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180669T>A , CM000676.2:g.50180669T>A	GRCh38
NC_000014.8:g.50647387T>A , CM000676.1:g.50647387T>A	GRCh37
NC_000014.7:g.49717137T>A	NCBI36
NG_051073.1:g.56025A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.872A>T MANE Select	ENSP00000216373.5:p.Asp291Val
ENST00000216373.9:c.872A>T	ENSP00000216373.5:p.Asp291Val
ENST00000543680.5:c.872A>T	ENSP00000445328.1:p.Asp291Val
NM_006939.2:c.872A>T	NP_008870.2:p.Asp291Val
XM_005268021.1:c.692A>T	XP_005268078.1:p.Asp231Val
XM_011537103.1:c.833A>T	XP_011535405.1:p.Asp278Val
XM_011537104.1:c.872A>T	XP_011535406.1:p.Asp291Val
XR_943842.1:n.954-3118T>A
XR_943843.1:n.954-3118T>A
NM_006939.3:c.872A>T	NP_008870.2:p.Asp291Val
NM_006939.4:c.872A>T MANE Select	NP_008870.2:p.Asp291Val