Canonical Allele Identifier: CA706556879

Gene: SOS2

Linked Data

• dbSNP Id: rs1258410257
• MyVariant Identifiers: chr14:g.50616964_50616965del (hg19) ; chr14:g.50150246_50150247del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50150247_50150248del , CM000676.2:g.50150247_50150248del	GRCh38
NC_000014.8:g.50616965_50616966del , CM000676.1:g.50616965_50616966del	GRCh37
NC_000014.7:g.49686715_49686716del	NCBI36
NG_051073.1:g.86447_86448del

Transcript Alleles

HGVS	Amino-acid change
ENST00000216373.10:c.2162-17_2162-16del MANE Select	ENSP00000216373.5:n.2162-17_2162-16del
ENST00000216373.9:c.2162-17_2162-16del	ENSP00000216373.5:n.2162-17_2162-16del
ENST00000543680.5:c.2063-17_2063-16del	ENSP00000445328.1:n.2063-17_2063-16del
NM_006939.2:c.2162-17_2162-16del	NP_008870.2:n.2162-17_2162-16del
XM_005268021.1:c.1982-17_1982-16del	XP_005268078.1:n.1982-17_1982-16del
XM_011537103.1:c.2123-17_2123-16del	XP_011535405.1:n.2123-17_2123-16del
XM_011537104.1:c.2162-17_2162-16del	XP_011535406.1:n.2162-17_2162-16del
NM_006939.3:c.2162-17_2162-16del	NP_008870.2:n.2162-17_2162-16del
NM_006939.4:c.2162-17_2162-16del MANE Select	NP_008870.2:n.2162-17_2162-16del