Canonical Allele Identifier: CA2658529240

Gene: SPAST

Linked Data

• gnomAD v4: 2-32136856-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32136856T>C , CM000664.2:g.32136856T>C	GRCh38
NC_000002.11:g.32361925T>C , CM000664.1:g.32361925T>C	GRCh37
NC_000002.10:g.32215429T>C	NCBI36
NG_008730.1:g.78246T>C , LRG_714:g.78246T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*982-21T>C	ENSP00000515816.1:n.*982-21T>C
ENST00000315285.9:c.1322-21T>C MANE Select	ENSP00000320885.3:n.1322-21T>C
ENST00000621856.2:c.1319-21T>C	ENSP00000482496.2:n.1319-21T>C
ENST00000642281.1:c.1059-21T>C
ENST00000642455.1:c.1223-21T>C	ENSP00000493827.1:n.1223-21T>C
ENST00000642751.1:c.1096-21T>C
ENST00000642999.1:c.1064-21T>C	ENSP00000496589.1:n.1064-21T>C
ENST00000643327.1:c.480+218T>C
ENST00000643334.1:c.902-21T>C
ENST00000644408.1:c.1198-21T>C
ENST00000644954.1:c.968-21T>C	ENSP00000494312.1:n.968-21T>C
ENST00000645159.1:n.2059-21T>C
ENST00000645671.1:c.772-21T>C
ENST00000645730.1:c.593-253T>C
ENST00000646082.1:c.968-21T>C
ENST00000646571.1:c.1226-21T>C	ENSP00000495015.1:n.1226-21T>C
ENST00000647007.1:n.1014-21T>C
ENST00000647133.1:c.822-21T>C
ENST00000315285.7:c.1322-21T>C	ENSP00000320885.3:n.1322-21T>C
ENST00000345662.5:c.1226-21T>C	ENSP00000340817.1:n.1226-21T>C
ENST00000615843.4:c.1322-21T>C	ENSP00000480893.1:n.1322-21T>C
ENST00000621856.1:c.1064-21T>C	ENSP00000482496.1:n.1064-21T>C
NM_014946.3:c.1322-21T>C , LRG_714t1:c.1322-21T>C	NP_055761.2:n.1322-21T>C
NM_199436.1:c.1226-21T>C	NP_955468.1:n.1226-21T>C
XM_005264516.3:c.1319-21T>C	XP_005264573.1:n.1319-21T>C
XM_011533067.1:c.1322-21T>C	XP_011531369.1:n.1322-21T>C
NM_001363823.1:c.1319-21T>C	NP_001350752.1:n.1319-21T>C
NM_001363875.1:c.1223-21T>C	NP_001350804.1:n.1223-21T>C
XM_005264516.5:c.1319-21T>C	XP_005264573.1:n.1319-21T>C
XM_011533067.2:c.1322-21T>C	XP_011531369.1:n.1322-21T>C
XM_017004778.2:c.1226-21T>C	XP_016860267.1:n.1226-21T>C
NM_001363823.2:c.1319-21T>C	NP_001350752.1:n.1319-21T>C
NM_001363875.2:c.1223-21T>C	NP_001350804.1:n.1223-21T>C
NM_001377959.1:c.1226-21T>C	NP_001364888.1:n.1226-21T>C
NM_014946.4:c.1322-21T>C MANE Select	NP_055761.2:n.1322-21T>C
NM_199436.2:c.1226-21T>C	NP_955468.1:n.1226-21T>C