Canonical Allele Identifier: CA2831387916

Gene: SMN1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.70945880G>C , CM000667.2:g.70945880G>C	GRCh38
NC_000005.9:g.70241707G>C , CM000667.1:g.70241707G>C	GRCh37
NC_000005.8:g.70277463G>C	NCBI36
NG_008691.1:g.25940G>C , LRG_676:g.25940G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380707.9:c.724-186G>C MANE Select	ENSP00000370083.4:n.724-186G>C
ENST00000351205.8:c.724-186G>C	ENSP00000305857.5:n.724-186G>C
ENST00000380707.8:c.724-186G>C	ENSP00000370083.4:n.724-186G>C
ENST00000503079.6:c.628-186G>C	ENSP00000428128.1:n.628-186G>C
ENST00000506163.5:c.724-186G>C	ENSP00000424926.1:n.724-186G>C
ENST00000506239.6:c.724-186G>C	ENSP00000422679.2:n.724-186G>C
ENST00000507905.6:c.418-186G>C	ENSP00000430657.1:n.418-186G>C
ENST00000513228.1:n.291-186G>C
ENST00000514951.5:c.523-186G>C	ENSP00000423298.1:n.523-186G>C
ENST00000518504.5:n.241-186G>C
ENST00000625245.2:c.724-186G>C	ENSP00000486539.1:n.724-186G>C
NM_000344.3:c.724-186G>C , LRG_676t1:c.724-186G>C	NP_000335.1:n.724-186G>C
NM_001297715.1:c.724-186G>C	NP_001284644.1:n.724-186G>C
NM_022874.2:c.628-186G>C	NP_075012.1:n.628-186G>C
XM_011543596.1:c.724-186G>C	XP_011541898.1:n.724-186G>C
XM_011543597.1:c.523-186G>C	XP_011541899.1:n.523-186G>C
XM_011543598.1:c.427-186G>C	XP_011541900.1:n.427-186G>C
XM_011543598.3:c.427-186G>C	XP_011541900.1:n.427-186G>C
XM_017009786.1:c.628-186G>C	XP_016865275.1:n.628-186G>C
NM_000344.4:c.724-186G>C MANE Select	NP_000335.1:n.724-186G>C