Canonical Allele Identifier: CA1242461500
Gene: SPAST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32063752A= , CM000664.2:g.32063752A= GRCh38
NC_000002.11:g.32288821A= , CM000664.1:g.32288821A= GRCh37
NC_000002.10:g.32142325A= NCBI36
NG_008730.1:g.5142A= , LRG_714:g.5142A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.-80A= ENSP00000515816.1:n.-80A=
ENST00000315285.9:c.-80A= MANE Select ENSP00000320885.3:n.-80A=
ENST00000646571.1:c.-80A= ENSP00000495015.1:n.-80A=
ENST00000315285.7:c.-80A= ENSP00000320885.3:n.-80A=
ENST00000345662.5:c.-80A= ENSP00000340817.1:n.-80A=
ENST00000615843.4:c.-80A= ENSP00000480893.1:n.-80A=
NM_014946.3:c.-80A= , LRG_714t1:c.-80A= NP_055761.2:n.-80A=
NM_199436.1:c.-80A= NP_955468.1:n.-80A=
XM_005264516.3:c.-80A= XP_005264573.1:n.-80A=
XM_011533067.1:c.-80A= XP_011531369.1:n.-80A=
NM_001363823.1:c.-80A= NP_001350752.1:n.-80A=
NM_001363875.1:c.-80A= NP_001350804.1:n.-80A=
XM_011533067.2:c.-80A= XP_011531369.1:n.-80A=
XM_017004778.2:c.-80A= XP_016860267.1:n.-80A=
NM_001363823.2:c.-80A= NP_001350752.1:n.-80A=
NM_001363875.2:c.-80A= NP_001350804.1:n.-80A=
NM_001377959.1:c.-80A= NP_001364888.1:n.-80A=
NM_014946.4:c.-80A= MANE Select NP_055761.2:n.-80A=
NM_199436.2:c.-80A= NP_955468.1:n.-80A=