Canonical Allele Identifier: CA360096895

Gene: SMN1

Linked Data

• MyVariant Identifiers: chr5:g.70241944G>A (hg19) ; chr5:g.70946117G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.70946117G>A , CM000667.2:g.70946117G>A	GRCh38
NC_000005.9:g.70241944G>A , CM000667.1:g.70241944G>A	GRCh37
NC_000005.8:g.70277700G>A	NCBI36
NG_008691.1:g.26177G>A , LRG_676:g.26177G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380707.9:c.775G>A MANE Select	ENSP00000370083.4:p.Ala259Thr
ENST00000351205.8:c.775G>A	ENSP00000305857.5:p.Ala259Thr
ENST00000380707.8:c.775G>A	ENSP00000370083.4:p.Ala259Thr
ENST00000503079.6:c.679G>A	ENSP00000428128.1:p.Ala227Thr
ENST00000506163.5:c.775G>A	ENSP00000424926.1:p.Ala259Thr
ENST00000506239.6:c.775G>A	ENSP00000422679.2:p.Ala259Thr
ENST00000510679.1:n.29G>A
ENST00000513228.1:n.342G>A
ENST00000514951.5:c.574G>A	ENSP00000423298.1:p.Ala192Thr
ENST00000518504.5:n.292G>A
ENST00000625245.2:c.775G>A	ENSP00000486539.1:p.Ala259Thr
NM_000344.3:c.775G>A , LRG_676t1:c.775G>A	NP_000335.1:p.Ala259Thr
NM_001297715.1:c.775G>A	NP_001284644.1:p.Ala259Thr
NM_022874.2:c.679G>A	NP_075012.1:p.Ala227Thr
XM_011543596.1:c.775G>A	XP_011541898.1:p.Ala259Thr
XM_011543597.1:c.574G>A	XP_011541899.1:p.Ala192Thr
XM_011543598.1:c.478G>A	XP_011541900.1:p.Ala160Thr
XM_011543598.3:c.478G>A	XP_011541900.1:p.Ala160Thr
XM_017009786.1:c.679G>A	XP_016865275.1:p.Ala227Thr
NM_000344.4:c.775G>A MANE Select	NP_000335.1:p.Ala259Thr