Canonical Allele Identifier: CA389649644

Gene: SOS2

Linked Data

• COSMIC: COSM4816568 ; COSM4816569
• MyVariant Identifiers: chr14:g.50666501C>G (hg19) ; chr14:g.50199783C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50199783C>G , CM000676.2:g.50199783C>G	GRCh38
NC_000014.8:g.50666501C>G , CM000676.1:g.50666501C>G	GRCh37
NC_000014.7:g.49736251C>G	NCBI36
NG_051073.1:g.36911G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.418G>C MANE Select	ENSP00000216373.5:p.Asp140His
ENST00000216373.9:c.418G>C	ENSP00000216373.5:p.Asp140His
ENST00000543680.5:c.418G>C	ENSP00000445328.1:p.Asp140His
ENST00000555666.1:n.597G>C
ENST00000556469.5:n.389G>C
NM_006939.2:c.418G>C	NP_008870.2:p.Asp140His
XM_005268021.1:c.238G>C	XP_005268078.1:p.Asp80His
XM_011537103.1:c.379G>C	XP_011535405.1:p.Asp127His
XM_011537104.1:c.418G>C	XP_011535406.1:p.Asp140His
XR_943842.1:n.1039+15911C>G
XR_943843.1:n.1039+15911C>G
NM_006939.3:c.418G>C	NP_008870.2:p.Asp140His
NM_006939.4:c.418G>C MANE Select	NP_008870.2:p.Asp140His