Canonical Allele Identifier: CA2624772222

Gene: SOS2

Linked Data

• gnomAD v4: 14-50180558-C-CAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180560_50180561insAAAA , CM000676.2:g.50180560_50180561insAAAA	GRCh38
NC_000014.8:g.50647278_50647279insAAAA , CM000676.1:g.50647278_50647279insAAAA	GRCh37
NC_000014.7:g.49717028_49717029insAAAA	NCBI36
NG_051073.1:g.56135_56136insTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.969+13_969+14insTTTT MANE Select	ENSP00000216373.5:n.969+13_969+14insTTTT
ENST00000216373.9:c.969+13_969+14insTTTT	ENSP00000216373.5:n.969+13_969+14insTTTT
ENST00000543680.5:c.969+13_969+14insTTTT	ENSP00000445328.1:n.969+13_969+14insTTTT
ENST00000555794.2:c.83+13_83+14insTTTT
NM_006939.2:c.969+13_969+14insTTTT	NP_008870.2:n.969+13_969+14insTTTT
XM_005268021.1:c.789+13_789+14insTTTT	XP_005268078.1:n.789+13_789+14insTTTT
XM_011537103.1:c.930+13_930+14insTTTT	XP_011535405.1:n.930+13_930+14insTTTT
XM_011537104.1:c.969+13_969+14insTTTT	XP_011535406.1:n.969+13_969+14insTTTT
XR_943842.1:n.954-3227_954-3226insAAAA
XR_943843.1:n.954-3227_954-3226insAAAA
NM_006939.3:c.969+13_969+14insTTTT	NP_008870.2:n.969+13_969+14insTTTT
NM_006939.4:c.969+13_969+14insTTTT MANE Select	NP_008870.2:n.969+13_969+14insTTTT