Canonical Allele Identifier: CA10620860

Gene: SH3BP2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.2820698G>T , CM000666.2:g.2820698G>T	GRCh38
NC_000004.11:g.2822425G>T , CM000666.1:g.2822425G>T	GRCh37
NC_000004.10:g.2792223G>T	NCBI36
NG_011609.1:g.32676G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001122681.2:c.81G>T MANE Select	NP_001116153.1:p.Val27=
ENST00000503393.8:c.81G>T MANE Select	ENSP00000422168.3:p.Val27=
NM_001122681.1:c.81G>T	NP_001116153.1:p.Val27=
NM_001145855.1:c.165G>T	NP_001139327.1:p.Val55=
NM_001145855.2:c.165G>T	NP_001139327.1:p.Val55=
NM_001145856.1:c.252G>T	NP_001139328.1:p.Val84=
NM_001145856.2:c.252G>T	NP_001139328.1:p.Val84=
NM_003023.4:c.81G>T	NP_003014.3:p.Val27=
ENST00000356331.9:c.81G>T	ENSP00000348685.5:p.Val27=
ENST00000435136.6:c.81G>T	ENSP00000403231.2:p.Val27=
ENST00000435136.8:c.165G>T	ENSP00000403231.3:p.Val55=
ENST00000442312.6:c.165G>T	ENSP00000388152.2:p.Val55=
ENST00000452765.6:c.81G>T	ENSP00000409746.2:p.Val27=
ENST00000502260.5:c.81G>T	ENSP00000425537.1:p.Val27=
ENST00000503219.5:c.81G>T	ENSP00000422796.1:p.Val27=
ENST00000503393.6:c.252G>T	ENSP00000422168.2:p.Val84=
ENST00000504294.5:c.81G>T	ENSP00000423275.1:p.Val27=
ENST00000506932.1:n.30G>T
ENST00000508385.5:c.81G>T	ENSP00000424917.1:p.Val27=
ENST00000509677.5:n.440G>T
ENST00000510074.5:n.189G>T
ENST00000511185.5:n.262G>T
ENST00000511237.5:n.189G>T
ENST00000511663.5:n.136G>T
ENST00000511747.5:c.81G>T	ENSP00000424846.1:p.Val27=
ENST00000511747.6:c.252G>T	ENSP00000424846.2:p.Val84=
ENST00000512014.5:c.81G>T	ENSP00000424105.1:p.Val27=
ENST00000512131.5:n.152G>T
ENST00000513020.5:c.81G>T	ENSP00000424072.1:p.Val27=
ENST00000513095.5:c.81G>T	ENSP00000423823.1:p.Val27=
ENST00000515737.5:c.81G>T	ENSP00000422605.1:p.Val27=
XM_005247998.3:c.90G>T	XP_005248055.1:p.Val30=
XM_005247999.3:c.81G>T	XP_005248056.1:p.Val27=
XM_011513547.1:c.252G>T	XP_011511849.1:p.Val84=
XM_011513548.1:c.81G>T	XP_011511850.1:p.Val27=
XM_011513549.1:c.81G>T	XP_011511851.1:p.Val27=
XM_011513550.1:c.81G>T	XP_011511852.1:p.Val27=
XM_011513551.1:c.81G>T	XP_011511853.1:p.Val27=
XM_011513552.1:c.-266G>T	XP_011511854.1:n.-266G>T
XM_011513553.1:c.-678G>T	XP_011511855.1:n.-678G>T
XM_011513554.1:c.81G>T	XP_011511856.1:p.Val27=
XM_011513555.1:c.81G>T	XP_011511857.1:p.Val27=
XM_011513556.1:c.81G>T	XP_011511858.1:p.Val27=
XR_924990.1:n.85G>T