Canonical Allele Identifier: CA392218346

Gene: SPG11

Linked Data

• MyVariant Identifiers: chr15:g.44865870T>A (hg19) ; chr15:g.44573672T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44573672T>A , CM000677.2:g.44573672T>A	GRCh38
NC_000015.9:g.44865870T>A , CM000677.1:g.44865870T>A	GRCh37
NC_000015.8:g.42653162T>A	NCBI36
NG_008885.1:g.95007A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.5867-3014A>T	ENSP00000453246.2:n.5867-3014A>T
ENST00000561391.2:n.2308A>T
ENST00000682065.1:c.5936A>T	ENSP00000507025.1:p.Gln1979Leu
ENST00000682460.1:c.*2337A>T	ENSP00000508334.1:n.*2337A>T
ENST00000682495.1:c.*2572A>T	ENSP00000507166.1:n.*2572A>T
ENST00000682669.1:c.5879A>T	ENSP00000507782.1:p.Gln1960Leu
ENST00000683186.1:c.*2843A>T	ENSP00000507268.1:n.*2843A>T
ENST00000683496.1:c.6006+1230A>T	ENSP00000506968.1:n.6006+1230A>T
ENST00000683734.1:c.*30A>T	ENSP00000508319.1:n.*30A>T
ENST00000683753.1:n.5126A>T
ENST00000684038.1:c.*2500A>T	ENSP00000507141.1:n.*2500A>T
ENST00000684235.1:c.6080A>T	ENSP00000508295.1:p.Gln2027Leu
ENST00000684676.1:c.*229A>T	ENSP00000506948.1:n.*229A>T
ENST00000261866.12:c.6080A>T MANE Select	ENSP00000261866.7:p.Gln2027Leu
ENST00000261866.11:c.6080A>T	ENSP00000261866.7:p.Gln2027Leu
ENST00000427534.6:c.6080A>T	ENSP00000396110.2:p.Gln2027Leu
ENST00000535302.6:c.5867-852A>T	ENSP00000445278.2:n.5867-852A>T
ENST00000558080.1:n.445A>T
ENST00000558319.5:c.6080A>T	ENSP00000453599.1:p.Gln2027Leu
ENST00000559511.5:c.715-3014A>T
ENST00000559933.1:n.149A>T
ENST00000561268.5:n.12A>T
NM_001160227.1:c.5867-852A>T	NP_001153699.1:n.5867-852A>T
NM_025137.3:c.6080A>T	NP_079413.3:p.Gln2027Leu
XM_005254695.3:c.5822A>T	XP_005254752.1:p.Gln1941Leu
XM_006720700.1:c.5936A>T	XP_006720763.1:p.Gln1979Leu
XM_017022634.1:c.6080A>T	XP_016878123.1:p.Gln2027Leu
XM_017022636.1:c.2957A>T	XP_016878125.1:p.Gln986Leu
NM_025137.4:c.6080A>T MANE Select	NP_079413.3:p.Gln2027Leu
NM_001160227.2:c.5867-852A>T	NP_001153699.1:n.5867-852A>T