Canonical Allele Identifier: CA2511870057

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50152753_50152754del , CM000676.2:g.50152753_50152754del	GRCh38
NC_000014.8:g.50619471_50619472del , CM000676.1:g.50619471_50619472del	GRCh37
NC_000014.7:g.49689221_49689222del	NCBI36
NG_051073.1:g.83940_83941del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.2161+316_2161+317del MANE Select	ENSP00000216373.5:n.2161+316_2161+317del
ENST00000216373.9:c.2161+316_2161+317del	ENSP00000216373.5:n.2161+316_2161+317del
ENST00000543680.5:c.2062+316_2062+317del	ENSP00000445328.1:n.2062+316_2062+317del
NM_006939.2:c.2161+316_2161+317del	NP_008870.2:n.2161+316_2161+317del
XM_005268021.1:c.1981+316_1981+317del	XP_005268078.1:n.1981+316_1981+317del
XM_011537103.1:c.2122+316_2122+317del	XP_011535405.1:n.2122+316_2122+317del
XM_011537104.1:c.2161+316_2161+317del	XP_011535406.1:n.2161+316_2161+317del
NM_006939.3:c.2161+316_2161+317del	NP_008870.2:n.2161+316_2161+317del
NM_006939.4:c.2161+316_2161+317del MANE Select	NP_008870.2:n.2161+316_2161+317del