Canonical Allele Identifier: CA392218328

Gene: SPG11

Linked Data

• MyVariant Identifiers: chr15:g.44865862C>T (hg19) ; chr15:g.44573664C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44573664C>T , CM000677.2:g.44573664C>T	GRCh38
NC_000015.9:g.44865862C>T , CM000677.1:g.44865862C>T	GRCh37
NC_000015.8:g.42653154C>T	NCBI36
NG_008885.1:g.95015G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.5867-3006G>A	ENSP00000453246.2:n.5867-3006G>A
ENST00000561391.2:n.2316G>A
ENST00000682065.1:c.5944G>A	ENSP00000507025.1:p.Asp1982Asn
ENST00000682460.1:c.*2345G>A	ENSP00000508334.1:n.*2345G>A
ENST00000682495.1:c.*2580G>A	ENSP00000507166.1:n.*2580G>A
ENST00000682669.1:c.5887G>A	ENSP00000507782.1:p.Asp1963Asn
ENST00000683186.1:c.*2851G>A	ENSP00000507268.1:n.*2851G>A
ENST00000683496.1:c.6006+1238G>A	ENSP00000506968.1:n.6006+1238G>A
ENST00000683734.1:c.*38G>A	ENSP00000508319.1:n.*38G>A
ENST00000683753.1:n.5134G>A
ENST00000684038.1:c.*2508G>A	ENSP00000507141.1:n.*2508G>A
ENST00000684235.1:c.6088G>A	ENSP00000508295.1:p.Asp2030Asn
ENST00000684676.1:c.*237G>A	ENSP00000506948.1:n.*237G>A
ENST00000261866.12:c.6088G>A MANE Select	ENSP00000261866.7:p.Asp2030Asn
ENST00000261866.11:c.6088G>A	ENSP00000261866.7:p.Asp2030Asn
ENST00000427534.6:c.6088G>A	ENSP00000396110.2:p.Asp2030Asn
ENST00000535302.6:c.5867-844G>A	ENSP00000445278.2:n.5867-844G>A
ENST00000558080.1:n.453G>A
ENST00000558319.5:c.6088G>A	ENSP00000453599.1:p.Asp2030Asn
ENST00000559511.5:c.715-3006G>A
ENST00000559933.1:n.157G>A
ENST00000561268.5:n.20G>A
NM_001160227.1:c.5867-844G>A	NP_001153699.1:n.5867-844G>A
NM_025137.3:c.6088G>A	NP_079413.3:p.Asp2030Asn
XM_005254695.3:c.5830G>A	XP_005254752.1:p.Asp1944Asn
XM_006720700.1:c.5944G>A	XP_006720763.1:p.Asp1982Asn
XM_017022634.1:c.6088G>A	XP_016878123.1:p.Asp2030Asn
XM_017022636.1:c.2965G>A	XP_016878125.1:p.Asp989Asn
NM_025137.4:c.6088G>A MANE Select	NP_079413.3:p.Asp2030Asn
NM_001160227.2:c.5867-844G>A	NP_001153699.1:n.5867-844G>A