Canonical Allele Identifier: CA389649607
Gene: SOS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50199768C>A , CM000676.2:g.50199768C>A GRCh38
NC_000014.8:g.50666486C>A , CM000676.1:g.50666486C>A GRCh37
NC_000014.7:g.49736236C>A NCBI36
NG_051073.1:g.36926G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000216373.10:c.433G>T MANE Select ENSP00000216373.5:p.Ala145Ser
ENST00000216373.9:c.433G>T ENSP00000216373.5:p.Ala145Ser
ENST00000543680.5:c.433G>T ENSP00000445328.1:p.Ala145Ser
ENST00000555666.1:n.612G>T
ENST00000556469.5:n.404G>T
NM_006939.2:c.433G>T NP_008870.2:p.Ala145Ser
XM_005268021.1:c.253G>T XP_005268078.1:p.Ala85Ser
XM_011537103.1:c.394G>T XP_011535405.1:p.Ala132Ser
XM_011537104.1:c.433G>T XP_011535406.1:p.Ala145Ser
XR_943842.1:n.1039+15896C>A
XR_943843.1:n.1039+15896C>A
NM_006939.3:c.433G>T NP_008870.2:p.Ala145Ser
NM_006939.4:c.433G>T MANE Select NP_008870.2:p.Ala145Ser