Canonical Allele Identifier: CA646623145
Gene: SPAST HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32063791_32063792insT , CM000664.2:g.32063791_32063792insT GRCh38
NC_000002.11:g.32288860_32288861insT , CM000664.1:g.32288860_32288861insT GRCh37
NC_000002.10:g.32142364_32142365insT NCBI36
NG_008730.1:g.5181_5182insT , LRG_714:g.5181_5182insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.-41_-40insT ENSP00000515816.1:n.-41_-40insT
ENST00000315285.9:c.-41_-40insT MANE Select ENSP00000320885.3:n.-41_-40insT
ENST00000621856.2:c.-41_-40insT ENSP00000482496.2:n.-41_-40insT
ENST00000646571.1:c.-41_-40insT ENSP00000495015.1:n.-41_-40insT
ENST00000315285.7:c.-41_-40insT ENSP00000320885.3:n.-41_-40insT
ENST00000345662.5:c.-41_-40insT ENSP00000340817.1:n.-41_-40insT
ENST00000615843.4:c.-41_-40insT ENSP00000480893.1:n.-41_-40insT
NM_014946.3:c.-41_-40insT , LRG_714t1:c.-41_-40insT NP_055761.2:n.-41_-40insT
NM_199436.1:c.-41_-40insT NP_955468.1:n.-41_-40insT
XM_005264516.3:c.-41_-40insT XP_005264573.1:n.-41_-40insT
XM_011533067.1:c.-41_-40insT XP_011531369.1:n.-41_-40insT
NM_001363823.1:c.-41_-40insT NP_001350752.1:n.-41_-40insT
NM_001363875.1:c.-41_-40insT NP_001350804.1:n.-41_-40insT
XM_011533067.2:c.-41_-40insT XP_011531369.1:n.-41_-40insT
XM_017004778.2:c.-41_-40insT XP_016860267.1:n.-41_-40insT
NM_001363823.2:c.-41_-40insT NP_001350752.1:n.-41_-40insT
NM_001363875.2:c.-41_-40insT NP_001350804.1:n.-41_-40insT
NM_001377959.1:c.-41_-40insT NP_001364888.1:n.-41_-40insT
NM_014946.4:c.-41_-40insT MANE Select NP_055761.2:n.-41_-40insT
NM_199436.2:c.-41_-40insT NP_955468.1:n.-41_-40insT