Canonical Allele Identifier: CA2136058792

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50130497T= , CM000676.2:g.50130497T=	GRCh38
NC_000014.8:g.50597215T= , CM000676.1:g.50597215T=	GRCh37
NC_000014.7:g.49666965T=	NCBI36
NG_051073.1:g.106197A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000216373.10:c.3337+4A= MANE Select	ENSP00000216373.5:n.3337+4A=
ENST00000216373.9:c.3337+4A=	ENSP00000216373.5:n.3337+4A=
ENST00000543680.5:c.3238+4A=	ENSP00000445328.1:n.3238+4A=
NM_006939.2:c.3337+4A=	NP_008870.2:n.3337+4A=
XM_005268021.1:c.3157+4A=	XP_005268078.1:n.3157+4A=
XM_011537103.1:c.3298+4A=	XP_011535405.1:n.3298+4A=
NM_006939.3:c.3337+4A=	NP_008870.2:n.3337+4A=
NM_006939.4:c.3337+4A= MANE Select	NP_008870.2:n.3337+4A=