Canonical Allele Identifier: CA346504185

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32144952C>A , CM000664.2:g.32144952C>A	GRCh38
NC_000002.11:g.32370021C>A , CM000664.1:g.32370021C>A	GRCh37
NC_000002.10:g.32223525C>A	NCBI36
NG_008730.1:g.86342C>A , LRG_714:g.86342C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_014946.4:c.1632C>A MANE Select	NP_055761.2:p.Tyr544Ter
ENST00000315285.9:c.1632C>A MANE Select	ENSP00000320885.3:p.Tyr544Ter
NM_001363823.1:c.1629C>A	NP_001350752.1:p.Tyr543Ter
NM_001363823.2:c.1629C>A	NP_001350752.1:p.Tyr543Ter
NM_001363875.1:c.1533C>A	NP_001350804.1:p.Tyr511Ter
NM_001363875.2:c.1533C>A	NP_001350804.1:p.Tyr511Ter
NM_001377959.1:c.1520+1537C>A	NP_001364888.1:n.1520+1537C>A
NM_014946.3:c.1632C>A , LRG_714t1:c.1632C>A	NP_055761.2:p.Tyr544Ter
NM_199436.1:c.1536C>A	NP_955468.1:p.Tyr512Ter
NM_199436.2:c.1536C>A	NP_955468.1:p.Tyr512Ter
ENST00000315285.7:c.1632C>A	ENSP00000320885.3:p.Tyr544Ter
ENST00000345662.5:c.1536C>A	ENSP00000340817.1:p.Tyr512Ter
ENST00000615843.4:c.1632C>A	ENSP00000480893.1:p.Tyr544Ter
ENST00000621856.1:c.1374C>A	ENSP00000482496.1:p.Tyr458Ter
ENST00000621856.2:c.1629C>A	ENSP00000482496.2:p.Tyr543Ter
ENST00000642281.1:c.1369C>A
ENST00000642455.1:c.1533C>A	ENSP00000493827.1:p.Tyr511Ter
ENST00000642751.1:c.1390+1537C>A
ENST00000642999.1:c.1374C>A	ENSP00000496589.1:p.Tyr458Ter
ENST00000643334.1:c.1212C>A
ENST00000644408.1:c.1508C>A
ENST00000644954.1:c.1278C>A	ENSP00000494312.1:p.Tyr426Ter
ENST00000645159.1:n.2369C>A
ENST00000645671.1:c.1066+1537C>A
ENST00000645730.1:c.811C>A
ENST00000646082.1:c.1278C>A
ENST00000646571.1:c.1536C>A	ENSP00000495015.1:p.Tyr512Ter
ENST00000647007.1:n.1324C>A
ENST00000647133.1:c.1132C>A
ENST00000704289.1:c.*1292C>A	ENSP00000515816.1:n.*1292C>A
XM_005264516.3:c.1629C>A	XP_005264573.1:p.Tyr543Ter
XM_005264516.5:c.1629C>A	XP_005264573.1:p.Tyr543Ter
XM_011533067.1:c.1616+1537C>A	XP_011531369.1:n.1616+1537C>A
XM_011533067.2:c.1616+1537C>A	XP_011531369.1:n.1616+1537C>A
XM_017004778.2:c.1520+1537C>A	XP_016860267.1:n.1520+1537C>A