Canonical Allele Identifier: CA444975749

Gene: SMN1

Linked Data

• MyVariant Identifiers: chr5:g.70247779A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.70951952A>G , CM000667.2:g.70951952A>G	GRCh38
NC_000005.9:g.70247779A>G , CM000667.1:g.70247779A>G	GRCh37
NC_000005.8:g.70283535A>G	NCBI36
NG_008691.1:g.32012A>G , LRG_676:g.32012A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000380707.9:c.846A>G MANE Select	ENSP00000370083.4:p.Gln282=
ENST00000351205.8:c.846A>G	ENSP00000305857.5:p.Gln282=
ENST00000380707.8:c.846A>G	ENSP00000370083.4:p.Gln282=
ENST00000503079.6:c.750A>G	ENSP00000428128.1:p.Gln250=
ENST00000506163.5:c.835-487A>G	ENSP00000424926.1:n.835-487A>G
ENST00000506239.6:c.*59-487A>G	ENSP00000422679.2:n.*59-487A>G
ENST00000510679.1:n.100A>G
ENST00000514951.5:c.645A>G	ENSP00000423298.1:p.Gln215=
NM_000344.3:c.846A>G , LRG_676t1:c.846A>G	NP_000335.1:p.Gln282=
NM_001297715.1:c.835-487A>G	NP_001284644.1:n.835-487A>G
NM_022874.2:c.750A>G	NP_075012.1:p.Gln250=
XM_011543597.1:c.645A>G	XP_011541899.1:p.Gln215=
XM_011543598.1:c.549A>G	XP_011541900.1:p.Gln183=
XM_011543598.3:c.549A>G	XP_011541900.1:p.Gln183=
XM_017009786.1:c.739-487A>G	XP_016865275.1:n.739-487A>G
NM_000344.4:c.846A>G MANE Select	NP_000335.1:p.Gln282=