Canonical Allele Identifier: CA3111514636

Gene: SH3BP2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.2831587G= , CM000666.2:g.2831587G=	GRCh38
NC_000004.11:g.2833314G= , CM000666.1:g.2833314G=	GRCh37
NC_000004.10:g.2803112G=	NCBI36
NG_011609.1:g.43565G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435136.8:c.1342G=	ENSP00000403231.3:p.Gly448=
ENST00000503393.8:c.1258G= MANE Select	ENSP00000422168.3:p.Gly420=
ENST00000511747.6:c.1429G=	ENSP00000424846.2:p.Gly477=
ENST00000356331.9:c.1258G=	ENSP00000348685.5:p.Gly420=
ENST00000435136.6:c.1258G=	ENSP00000403231.2:p.Gly420=
ENST00000442312.6:c.1342G=	ENSP00000388152.2:p.Gly448=
ENST00000452765.6:c.1258G=	ENSP00000409746.2:p.Gly420=
ENST00000503393.6:c.1429G=	ENSP00000422168.2:p.Gly477=
ENST00000504450.1:n.555G=
ENST00000510204.5:n.1735G=
ENST00000511747.5:c.1258G=	ENSP00000424846.1:p.Gly420=
ENST00000513069.1:c.368G=
ENST00000515737.5:c.*1143G=	ENSP00000422605.1:n.*1143G=
ENST00000515802.5:n.1364G=
NM_001122681.1:c.1258G=	NP_001116153.1:p.Gly420=
NM_001145855.1:c.1342G=	NP_001139327.1:p.Gly448=
NM_001145856.1:c.1429G=	NP_001139328.1:p.Gly477=
NM_003023.4:c.1258G=	NP_003014.3:p.Gly420=
XM_005247998.3:c.1267G=	XP_005248055.1:p.Gly423=
XM_005247999.3:c.1258G=	XP_005248056.1:p.Gly420=
XM_011513547.1:c.1429G=	XP_011511849.1:p.Gly477=
XM_011513548.1:c.1258G=	XP_011511850.1:p.Gly420=
XM_011513549.1:c.1258G=	XP_011511851.1:p.Gly420=
XM_011513550.1:c.1258G=	XP_011511852.1:p.Gly420=
XM_011513551.1:c.1258G=	XP_011511853.1:p.Gly420=
XM_011513552.1:c.1087G=	XP_011511854.1:p.Gly363=
XM_011513553.1:c.895G=	XP_011511855.1:p.Gly299=
XM_011513554.1:c.603G=	XP_011511856.1:p.Met201=
XM_011513555.1:c.603G=	XP_011511857.1:p.Met201=
XM_011513556.1:c.603G=	XP_011511858.1:p.Met201=
XR_924990.1:n.1262G=
NM_001122681.2:c.1258G= MANE Select	NP_001116153.1:p.Gly420=
NM_001145855.2:c.1342G=	NP_001139327.1:p.Gly448=
NM_001145856.2:c.1429G=	NP_001139328.1:p.Gly477=