Canonical Allele Identifier: CA346601175
Gene: SPAST HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32063835A>C , CM000664.2:g.32063835A>C GRCh38
NC_000002.11:g.32288904A>C , CM000664.1:g.32288904A>C GRCh37
NC_000002.10:g.32142408A>C NCBI36
NG_008730.1:g.5225A>C , LRG_714:g.5225A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.4A>C ENSP00000515816.1:p.Asn2His
ENST00000315285.9:c.4A>C MANE Select ENSP00000320885.3:p.Asn2His
ENST00000621856.2:c.4A>C ENSP00000482496.2:p.Asn2His
ENST00000642455.1:c.4A>C ENSP00000493827.1:p.Asn2His
ENST00000646571.1:c.4A>C ENSP00000495015.1:p.Asn2His
ENST00000315285.7:c.4A>C ENSP00000320885.3:p.Asn2His
ENST00000345662.5:c.4A>C ENSP00000340817.1:p.Asn2His
ENST00000615843.4:c.4A>C ENSP00000480893.1:p.Asn2His
NM_014946.3:c.4A>C , LRG_714t1:c.4A>C NP_055761.2:p.Asn2His
NM_199436.1:c.4A>C NP_955468.1:p.Asn2His
XM_005264516.3:c.4A>C XP_005264573.1:p.Asn2His
XM_011533067.1:c.4A>C XP_011531369.1:p.Asn2His
NM_001363823.1:c.4A>C NP_001350752.1:p.Asn2His
NM_001363875.1:c.4A>C NP_001350804.1:p.Asn2His
XM_005264516.5:c.4A>C XP_005264573.1:p.Asn2His
XM_011533067.2:c.4A>C XP_011531369.1:p.Asn2His
XM_017004778.2:c.4A>C XP_016860267.1:p.Asn2His
NM_001363823.2:c.4A>C NP_001350752.1:p.Asn2His
NM_001363875.2:c.4A>C NP_001350804.1:p.Asn2His
NM_001377959.1:c.4A>C NP_001364888.1:p.Asn2His
NM_014946.4:c.4A>C MANE Select NP_055761.2:p.Asn2His
NM_199436.2:c.4A>C NP_955468.1:p.Asn2His