Canonical Allele Identifier: CA360096788

Gene: SMN1

Linked Data

• MyVariant Identifiers: chr5:g.70241930T>G (hg19) ; chr5:g.70946103T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.70946103T>G , CM000667.2:g.70946103T>G	GRCh38
NC_000005.9:g.70241930T>G , CM000667.1:g.70241930T>G	GRCh37
NC_000005.8:g.70277686T>G	NCBI36
NG_008691.1:g.26163T>G , LRG_676:g.26163T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380707.9:c.761T>G MANE Select	ENSP00000370083.4:p.Leu254Arg
ENST00000351205.8:c.761T>G	ENSP00000305857.5:p.Leu254Arg
ENST00000380707.8:c.761T>G	ENSP00000370083.4:p.Leu254Arg
ENST00000503079.6:c.665T>G	ENSP00000428128.1:p.Leu222Arg
ENST00000506163.5:c.761T>G	ENSP00000424926.1:p.Leu254Arg
ENST00000506239.6:c.761T>G	ENSP00000422679.2:p.Leu254Arg
ENST00000510679.1:n.15T>G
ENST00000513228.1:n.328T>G
ENST00000514951.5:c.560T>G	ENSP00000423298.1:p.Leu187Arg
ENST00000518504.5:n.278T>G
ENST00000625245.2:c.761T>G	ENSP00000486539.1:p.Leu254Arg
NM_000344.3:c.761T>G , LRG_676t1:c.761T>G	NP_000335.1:p.Leu254Arg
NM_001297715.1:c.761T>G	NP_001284644.1:p.Leu254Arg
NM_022874.2:c.665T>G	NP_075012.1:p.Leu222Arg
XM_011543596.1:c.761T>G	XP_011541898.1:p.Leu254Arg
XM_011543597.1:c.560T>G	XP_011541899.1:p.Leu187Arg
XM_011543598.1:c.464T>G	XP_011541900.1:p.Leu155Arg
XM_011543598.3:c.464T>G	XP_011541900.1:p.Leu155Arg
XM_017009786.1:c.665T>G	XP_016865275.1:p.Leu222Arg
NM_000344.4:c.761T>G MANE Select	NP_000335.1:p.Leu254Arg