Canonical Allele Identifier: CA425581450

Gene: SPAST

Linked Data

• gnomAD v4: 2-32089601-T-C
• MyVariant Identifiers: chr2:g.32314670T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32089601T>C , CM000664.2:g.32089601T>C	GRCh38
NC_000002.11:g.32314670T>C , CM000664.1:g.32314670T>C	GRCh37
NC_000002.10:g.32168174T>C	NCBI36
NG_008730.1:g.30991T>C , LRG_714:g.30991T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000704289.1:c.*242T>C	ENSP00000515816.1:n.*242T>C
ENST00000315285.9:c.582T>C MANE Select	ENSP00000320885.3:p.Leu194=
ENST00000621856.2:c.579T>C	ENSP00000482496.2:p.Leu193=
ENST00000642281.1:c.466T>C
ENST00000642455.1:c.579T>C	ENSP00000493827.1:p.Leu193=
ENST00000642751.1:c.452T>C
ENST00000642999.1:c.324T>C	ENSP00000496589.1:p.Leu108=
ENST00000643334.1:c.167T>C
ENST00000644408.1:c.458T>C
ENST00000644954.1:c.324T>C	ENSP00000494312.1:p.Leu108=
ENST00000645400.1:c.538T>C	ENSP00000496306.1:n.538T>C
ENST00000645671.1:c.37-9195T>C
ENST00000646082.1:c.416T>C
ENST00000646571.1:c.582T>C	ENSP00000495015.1:p.Leu194=
ENST00000647007.1:n.279T>C
ENST00000647133.1:c.157T>C
ENST00000315285.7:c.582T>C	ENSP00000320885.3:p.Leu194=
ENST00000345662.5:c.582T>C	ENSP00000340817.1:p.Leu194=
ENST00000615843.4:c.582T>C	ENSP00000480893.1:p.Leu194=
ENST00000621856.1:c.324T>C	ENSP00000482496.1:p.Leu108=
NM_014946.3:c.582T>C , LRG_714t1:c.582T>C	NP_055761.2:p.Leu194=
NM_199436.1:c.582T>C	NP_955468.1:p.Leu194=
XM_005264516.3:c.579T>C	XP_005264573.1:p.Leu193=
XM_011533067.1:c.582T>C	XP_011531369.1:p.Leu194=
NM_001363823.1:c.579T>C	NP_001350752.1:p.Leu193=
NM_001363875.1:c.579T>C	NP_001350804.1:p.Leu193=
XM_005264516.5:c.579T>C	XP_005264573.1:p.Leu193=
XM_011533067.2:c.582T>C	XP_011531369.1:p.Leu194=
XM_017004778.2:c.582T>C	XP_016860267.1:p.Leu194=
NM_001363823.2:c.579T>C	NP_001350752.1:p.Leu193=
NM_001363875.2:c.579T>C	NP_001350804.1:p.Leu193=
NM_001377959.1:c.582T>C	NP_001364888.1:p.Leu194=
NM_014946.4:c.582T>C MANE Select	NP_055761.2:p.Leu194=
NM_199436.2:c.582T>C	NP_955468.1:p.Leu194=