Canonical Allele Identifier: CA1554174018

Gene: SMN1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.70951775T= , CM000667.2:g.70951775T=	GRCh38
NC_000005.9:g.70247602T= , CM000667.1:g.70247602T=	GRCh37
NC_000005.8:g.70283358T=	NCBI36
NG_008691.1:g.31835T= , LRG_676:g.31835T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380707.9:c.835-166T= MANE Select	ENSP00000370083.4:n.835-166T=
ENST00000351205.8:c.835-166T=	ENSP00000305857.5:n.835-166T=
ENST00000380707.8:c.835-166T=	ENSP00000370083.4:n.835-166T=
ENST00000503079.6:c.739-166T=	ENSP00000428128.1:n.739-166T=
ENST00000506163.5:c.835-664T=	ENSP00000424926.1:n.835-664T=
ENST00000506239.6:c.*59-664T=	ENSP00000422679.2:n.*59-664T=
ENST00000510679.1:n.89-166T=
ENST00000514951.5:c.634-166T=	ENSP00000423298.1:n.634-166T=
NM_000344.3:c.835-166T= , LRG_676t1:c.835-166T=	NP_000335.1:n.835-166T=
NM_001297715.1:c.835-664T=	NP_001284644.1:n.835-664T=
NM_022874.2:c.739-166T=	NP_075012.1:n.739-166T=
XM_011543597.1:c.634-166T=	XP_011541899.1:n.634-166T=
XM_011543598.1:c.538-166T=	XP_011541900.1:n.538-166T=
XM_011543598.3:c.538-166T=	XP_011541900.1:n.538-166T=
XM_017009786.1:c.739-664T=	XP_016865275.1:n.739-664T=
NM_000344.4:c.835-166T= MANE Select	NP_000335.1:n.835-166T=