Canonical Allele Identifier: CA2699032436

Gene: SPAST

Linked Data

• dbSNP Id: rs2148684969

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32063771del , CM000664.2:g.32063771del	GRCh38
NC_000002.11:g.32288840del , CM000664.1:g.32288840del	GRCh37
NC_000002.10:g.32142344del	NCBI36
NG_008730.1:g.5161del , LRG_714:g.5161del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.-61del	ENSP00000515816.1:n.-61del
ENST00000315285.9:c.-61del MANE Select	ENSP00000320885.3:n.-61del
ENST00000646571.1:c.-61del	ENSP00000495015.1:n.-61del
ENST00000315285.7:c.-61del	ENSP00000320885.3:n.-61del
ENST00000345662.5:c.-61del	ENSP00000340817.1:n.-61del
ENST00000615843.4:c.-61del	ENSP00000480893.1:n.-61del
NM_014946.3:c.-61del , LRG_714t1:c.-61del	NP_055761.2:n.-61del
NM_199436.1:c.-61del	NP_955468.1:n.-61del
XM_005264516.3:c.-61del	XP_005264573.1:n.-61del
XM_011533067.1:c.-61del	XP_011531369.1:n.-61del
NM_001363823.1:c.-61del	NP_001350752.1:n.-61del
NM_001363875.1:c.-61del	NP_001350804.1:n.-61del
XM_011533067.2:c.-61del	XP_011531369.1:n.-61del
XM_017004778.2:c.-61del	XP_016860267.1:n.-61del
NM_001363823.2:c.-61del	NP_001350752.1:n.-61del
NM_001363875.2:c.-61del	NP_001350804.1:n.-61del
NM_001377959.1:c.-61del	NP_001364888.1:n.-61del
NM_014946.4:c.-61del MANE Select	NP_055761.2:n.-61del
NM_199436.2:c.-61del	NP_955468.1:n.-61del