Canonical Allele Identifier: CA1242501431

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32136838_32136839delinsTG , CM000664.2:g.32136838_32136839delinsTG	GRCh38
NC_000002.11:g.32361907_32361908delinsTG , CM000664.1:g.32361907_32361908delinsTG	GRCh37
NC_000002.10:g.32215411_32215412delinsTG	NCBI36
NG_008730.1:g.78228_78229delinsTG , LRG_714:g.78228_78229delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*982-39_*982-38delinsTG	ENSP00000515816.1:n.*982-39_*982-38delinsTG
ENST00000315285.9:c.1322-39_1322-38delinsTG MANE Select	ENSP00000320885.3:n.1322-39_1322-38delinsTG
ENST00000621856.2:c.1319-39_1319-38delinsTG	ENSP00000482496.2:n.1319-39_1319-38delinsTG
ENST00000642281.1:c.1059-39_1059-38delinsTG
ENST00000642455.1:c.1223-39_1223-38delinsTG	ENSP00000493827.1:n.1223-39_1223-38delinsTG
ENST00000642751.1:c.1096-39_1096-38delinsTG
ENST00000642999.1:c.1064-39_1064-38delinsTG	ENSP00000496589.1:n.1064-39_1064-38delinsTG
ENST00000643327.1:c.480+200_480+201delinsTG
ENST00000643334.1:c.902-39_902-38delinsTG
ENST00000644408.1:c.1198-39_1198-38delinsTG
ENST00000644954.1:c.968-39_968-38delinsTG	ENSP00000494312.1:n.968-39_968-38delinsTG
ENST00000645159.1:n.2059-39_2059-38delinsTG
ENST00000645671.1:c.772-39_772-38delinsTG
ENST00000645730.1:c.593-271_593-270delinsTG
ENST00000646082.1:c.968-39_968-38delinsTG
ENST00000646571.1:c.1226-39_1226-38delinsTG	ENSP00000495015.1:n.1226-39_1226-38delinsTG
ENST00000647007.1:n.1014-39_1014-38delinsTG
ENST00000647133.1:c.822-39_822-38delinsTG
ENST00000315285.7:c.1322-39_1322-38delinsTG	ENSP00000320885.3:n.1322-39_1322-38delinsTG
ENST00000345662.5:c.1226-39_1226-38delinsTG	ENSP00000340817.1:n.1226-39_1226-38delinsTG
ENST00000615843.4:c.1322-39_1322-38delinsTG	ENSP00000480893.1:n.1322-39_1322-38delinsTG
ENST00000621856.1:c.1064-39_1064-38delinsTG	ENSP00000482496.1:n.1064-39_1064-38delinsTG
NM_014946.3:c.1322-39_1322-38delinsTG , LRG_714t1:c.1322-39_1322-38delinsTG	NP_055761.2:n.1322-39_1322-38delinsTG
NM_199436.1:c.1226-39_1226-38delinsTG	NP_955468.1:n.1226-39_1226-38delinsTG
XM_005264516.3:c.1319-39_1319-38delinsTG	XP_005264573.1:n.1319-39_1319-38delinsTG
XM_011533067.1:c.1322-39_1322-38delinsTG	XP_011531369.1:n.1322-39_1322-38delinsTG
NM_001363823.1:c.1319-39_1319-38delinsTG	NP_001350752.1:n.1319-39_1319-38delinsTG
NM_001363875.1:c.1223-39_1223-38delinsTG	NP_001350804.1:n.1223-39_1223-38delinsTG
XM_005264516.5:c.1319-39_1319-38delinsTG	XP_005264573.1:n.1319-39_1319-38delinsTG
XM_011533067.2:c.1322-39_1322-38delinsTG	XP_011531369.1:n.1322-39_1322-38delinsTG
XM_017004778.2:c.1226-39_1226-38delinsTG	XP_016860267.1:n.1226-39_1226-38delinsTG
NM_001363823.2:c.1319-39_1319-38delinsTG	NP_001350752.1:n.1319-39_1319-38delinsTG
NM_001363875.2:c.1223-39_1223-38delinsTG	NP_001350804.1:n.1223-39_1223-38delinsTG
NM_001377959.1:c.1226-39_1226-38delinsTG	NP_001364888.1:n.1226-39_1226-38delinsTG
NM_014946.4:c.1322-39_1322-38delinsTG MANE Select	NP_055761.2:n.1322-39_1322-38delinsTG
NM_199436.2:c.1226-39_1226-38delinsTG	NP_955468.1:n.1226-39_1226-38delinsTG