Canonical Allele Identifier: CA1554174035

Gene: SMN1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.70951809T= , CM000667.2:g.70951809T=	GRCh38
NC_000005.9:g.70247636T= , CM000667.1:g.70247636T=	GRCh37
NC_000005.8:g.70283392T=	NCBI36
NG_008691.1:g.31869T= , LRG_676:g.31869T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380707.9:c.835-132T= MANE Select	ENSP00000370083.4:n.835-132T=
ENST00000351205.8:c.835-132T=	ENSP00000305857.5:n.835-132T=
ENST00000380707.8:c.835-132T=	ENSP00000370083.4:n.835-132T=
ENST00000503079.6:c.739-132T=	ENSP00000428128.1:n.739-132T=
ENST00000506163.5:c.835-630T=	ENSP00000424926.1:n.835-630T=
ENST00000506239.6:c.*59-630T=	ENSP00000422679.2:n.*59-630T=
ENST00000510679.1:n.89-132T=
ENST00000514951.5:c.634-132T=	ENSP00000423298.1:n.634-132T=
NM_000344.3:c.835-132T= , LRG_676t1:c.835-132T=	NP_000335.1:n.835-132T=
NM_001297715.1:c.835-630T=	NP_001284644.1:n.835-630T=
NM_022874.2:c.739-132T=	NP_075012.1:n.739-132T=
XM_011543597.1:c.634-132T=	XP_011541899.1:n.634-132T=
XM_011543598.1:c.538-132T=	XP_011541900.1:n.538-132T=
XM_011543598.3:c.538-132T=	XP_011541900.1:n.538-132T=
XM_017009786.1:c.739-630T=	XP_016865275.1:n.739-630T=
NM_000344.4:c.835-132T= MANE Select	NP_000335.1:n.835-132T=