Canonical Allele Identifier: CA1242501278
Gene: SPAST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32136647A= , CM000664.2:g.32136647A= GRCh38
NC_000002.11:g.32361716A= , CM000664.1:g.32361716A= GRCh37
NC_000002.10:g.32215220A= NCBI36
NG_008730.1:g.78037A= , LRG_714:g.78037A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.*981+9A= ENSP00000515816.1:n.*981+9A=
ENST00000315285.9:c.1321+9A= MANE Select ENSP00000320885.3:n.1321+9A=
ENST00000621856.2:c.1318+9A= ENSP00000482496.2:n.1318+9A=
ENST00000642281.1:c.1058+9A=
ENST00000642455.1:c.1222+9A= ENSP00000493827.1:n.1222+9A=
ENST00000642751.1:c.1095+9A=
ENST00000642999.1:c.1063+9A= ENSP00000496589.1:n.1063+9A=
ENST00000643327.1:c.480+9A=
ENST00000643334.1:c.901+9A=
ENST00000644408.1:c.1197+9A=
ENST00000644954.1:c.967+9A= ENSP00000494312.1:n.967+9A=
ENST00000645159.1:n.2058+9A=
ENST00000645671.1:c.771+9A=
ENST00000645730.1:c.593-462A=
ENST00000646082.1:c.967+9A=
ENST00000646571.1:c.1225+9A= ENSP00000495015.1:n.1225+9A=
ENST00000647007.1:n.1013+9A=
ENST00000647133.1:c.821+9A=
ENST00000315285.7:c.1321+9A= ENSP00000320885.3:n.1321+9A=
ENST00000345662.5:c.1225+9A= ENSP00000340817.1:n.1225+9A=
ENST00000615843.4:c.1321+9A= ENSP00000480893.1:n.1321+9A=
ENST00000621856.1:c.1063+9A= ENSP00000482496.1:n.1063+9A=
NM_014946.3:c.1321+9A= , LRG_714t1:c.1321+9A= NP_055761.2:n.1321+9A=
NM_199436.1:c.1225+9A= NP_955468.1:n.1225+9A=
XM_005264516.3:c.1318+9A= XP_005264573.1:n.1318+9A=
XM_011533067.1:c.1321+9A= XP_011531369.1:n.1321+9A=
NM_001363823.1:c.1318+9A= NP_001350752.1:n.1318+9A=
NM_001363875.1:c.1222+9A= NP_001350804.1:n.1222+9A=
XM_005264516.5:c.1318+9A= XP_005264573.1:n.1318+9A=
XM_011533067.2:c.1321+9A= XP_011531369.1:n.1321+9A=
XM_017004778.2:c.1225+9A= XP_016860267.1:n.1225+9A=
NM_001363823.2:c.1318+9A= NP_001350752.1:n.1318+9A=
NM_001363875.2:c.1222+9A= NP_001350804.1:n.1222+9A=
NM_001377959.1:c.1225+9A= NP_001364888.1:n.1225+9A=
NM_014946.4:c.1321+9A= MANE Select NP_055761.2:n.1321+9A=
NM_199436.2:c.1225+9A= NP_955468.1:n.1225+9A=