Canonical Allele Identifier: CA10575835
Gene: SPAST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32140511_32146752dup , CM000664.2:g.32140511_32146752dup GRCh38
NC_000002.11:g.32365580_32371821dup , CM000664.1:g.32365580_32371821dup GRCh37
NC_000002.10:g.32219084_32225325dup NCBI36
NG_008730.1:g.81901_88142dup , LRG_714:g.81901_88142dup

Transcript Alleles

HGVS Amino-acid change
ENST00000704289.1:c.*1154-1393_*1348-466dup
ENST00000315285.9:c.1494-1393_1688-466dup
ENST00000621856.2:c.1491-1393_1685-466dup
ENST00000642281.1:c.1231-1393_1425-466dup
ENST00000642455.1:c.1395-1393_1589-466dup
ENST00000642751.1:c.1268-1393_1391-466dup
ENST00000642999.1:c.1236-1393_1430-466dup
ENST00000643334.1:c.1074-1393_1268-466dup
ENST00000644408.1:c.1370-1393_1564-443dup
ENST00000644954.1:c.1140-1393_1334-466dup
ENST00000645159.1:n.2231-1393_2425-466dup
ENST00000645671.1:c.944-1393_1067-466dup
ENST00000645730.1:c.673-1393_867-466dup
ENST00000646082.1:c.1140-1393_1334-466dup
ENST00000646571.1:c.1398-1393_1592-466dup
ENST00000647007.1:n.1186-1393_1380-466dup
ENST00000647133.1:c.994-1393_1188-466dup
ENST00000315285.7:c.1494-1393_1688-466dup
ENST00000345662.5:c.1398-1393_1592-466dup
ENST00000615843.4:c.1494-1393_1688-466dup
ENST00000621856.1:c.1236-1393_1430-466dup
NM_014946.3:c.1494-1393_1688-466dup , LRG_714t1:c.1494-1393_1688-466dup
NM_199436.1:c.1398-1393_1592-466dup
XM_005264516.3:c.1491-1393_1685-466dup
XM_011533067.1:c.1494-1393_1617-466dup
NM_001363823.1:c.1491-1393_1685-466dup
NM_001363875.1:c.1395-1393_1589-466dup
XM_005264516.5:c.1491-1393_1685-466dup
XM_011533067.2:c.1494-1393_1617-466dup
XM_017004778.2:c.1398-1393_1521-466dup
NM_001363823.2:c.1491-1393_1685-466dup
NM_001363875.2:c.1395-1393_1589-466dup
NM_001377959.1:c.1398-1393_1521-466dup
NM_014946.4:c.1494-1393_1688-466dup
NM_199436.2:c.1398-1393_1592-466dup