Canonical Allele Identifier: CA2136094956

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50199908C= , CM000676.2:g.50199908C=	GRCh38
NC_000014.8:g.50666626C= , CM000676.1:g.50666626C=	GRCh37
NC_000014.7:g.49736376C=	NCBI36
NG_051073.1:g.36786G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.346-53G= MANE Select	ENSP00000216373.5:n.346-53G=
ENST00000216373.9:c.346-53G=	ENSP00000216373.5:n.346-53G=
ENST00000543680.5:c.346-53G=	ENSP00000445328.1:n.346-53G=
ENST00000555666.1:n.525-53G=
ENST00000556469.5:n.317-53G=
NM_006939.2:c.346-53G=	NP_008870.2:n.346-53G=
XM_005268021.1:c.166-53G=	XP_005268078.1:n.166-53G=
XM_011537103.1:c.307-53G=	XP_011535405.1:n.307-53G=
XM_011537104.1:c.346-53G=	XP_011535406.1:n.346-53G=
XR_943842.1:n.1039+16036C=
XR_943843.1:n.1039+16036C=
NM_006939.3:c.346-53G=	NP_008870.2:n.346-53G=
NM_006939.4:c.346-53G= MANE Select	NP_008870.2:n.346-53G=