Canonical Allele Identifier: CA2173701356
Gene: SPG11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44598835T= , CM000677.2:g.44598835T= GRCh38
NC_000015.9:g.44891033T= , CM000677.1:g.44891033T= GRCh37
NC_000015.8:g.42678325T= NCBI36
NG_008885.1:g.69844A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559511.6:c.3688A= ENSP00000453246.2:p.Ile1230=
ENST00000682065.1:c.3688A= ENSP00000507025.1:p.Ile1230=
ENST00000682460.1:c.*108A= ENSP00000508334.1:n.*108A=
ENST00000682495.1:c.*180A= ENSP00000507166.1:n.*180A=
ENST00000682669.1:c.3487A= ENSP00000507782.1:p.Ile1163=
ENST00000682788.1:c.3688A= ENSP00000508089.1:p.Ile1230=
ENST00000682915.1:c.3781A= ENSP00000507493.1:n.3781A=
ENST00000683121.1:c.3688A= ENSP00000507557.1:p.Ile1230=
ENST00000683186.1:c.*451A= ENSP00000507268.1:n.*451A=
ENST00000683496.1:c.3688A= ENSP00000506968.1:p.Ile1230=
ENST00000683734.1:c.3688A= ENSP00000508319.1:p.Ile1230=
ENST00000683753.1:n.2734A=
ENST00000683838.1:n.762A=
ENST00000684038.1:c.*108A= ENSP00000507141.1:n.*108A=
ENST00000684235.1:c.3688A= ENSP00000508295.1:p.Ile1230=
ENST00000684676.1:c.3688A= ENSP00000506948.1:p.Ile1230=
ENST00000261866.12:c.3688A= MANE Select ENSP00000261866.7:p.Ile1230=
ENST00000261866.11:c.3688A= ENSP00000261866.7:p.Ile1230=
ENST00000427534.6:c.3688A= ENSP00000396110.2:p.Ile1230=
ENST00000535302.6:c.3688A= ENSP00000445278.2:p.Ile1230=
ENST00000558093.1:n.302A=
ENST00000558319.5:c.3688A= ENSP00000453599.1:p.Ile1230=
NM_001160227.1:c.3688A= NP_001153699.1:p.Ile1230=
NM_025137.3:c.3688A= NP_079413.3:p.Ile1230=
XM_005254695.3:c.3430A= XP_005254752.1:p.Ile1144=
XM_006720700.1:c.3688A= XP_006720763.1:p.Ile1230=
XM_006720701.2:c.3688A= XP_006720764.1:p.Ile1230=
XM_011522093.1:c.3687-462A= XP_011520395.1:n.3687-462A=
XR_931917.1:n.3719A=
XM_006720701.3:c.3688A= XP_006720764.1:p.Ile1230=
XM_017022634.1:c.3688A= XP_016878123.1:p.Ile1230=
XM_017022635.2:c.3688A= XP_016878124.1:p.Ile1230=
XM_017022636.1:c.565A= XP_016878125.1:p.Ile189=
XR_001751402.1:n.3718-462A=
XR_931917.2:n.3719A=
NM_025137.4:c.3688A= MANE Select NP_079413.3:p.Ile1230=
NM_001160227.2:c.3688A= NP_001153699.1:p.Ile1230=