Canonical Allele Identifier: CA1554170656

Gene: SMN1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.70925146_70925149delinsCAGG , CM000667.2:g.70925146_70925149delinsCAGG	GRCh38
NC_000005.9:g.70220973_70220976delinsCAGG , CM000667.1:g.70220973_70220976delinsCAGG	GRCh37
NC_000005.8:g.70256729_70256732delinsCAGG	NCBI36
NG_008691.1:g.5206_5209delinsCAGG , LRG_676:g.5206_5209delinsCAGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000380707.9:c.43_46delinsCAGG MANE Select	ENSP00000370083.4:p.Gln15=
ENST00000351205.8:c.43_46delinsCAGG	ENSP00000305857.5:p.Gln15=
ENST00000380707.8:c.43_46delinsCAGG	ENSP00000370083.4:p.Gln15=
ENST00000503079.6:c.43_46delinsCAGG	ENSP00000428128.1:p.Gln15=
ENST00000506163.5:c.43_46delinsCAGG	ENSP00000424926.1:p.Gln15=
ENST00000506239.6:c.43_46delinsCAGG	ENSP00000422679.2:p.Gln15=
ENST00000514951.5:c.43_46delinsCAGG	ENSP00000423298.1:p.Gln15=
ENST00000625245.2:c.43_46delinsCAGG	ENSP00000486539.1:p.Gln15=
NM_000344.3:c.43_46delinsCAGG , LRG_676t1:c.43_46delinsCAGG	NP_000335.1:p.Gln15=
NM_001297715.1:c.43_46delinsCAGG	NP_001284644.1:p.Gln15=
NM_022874.2:c.43_46delinsCAGG	NP_075012.1:p.Gln15=
XM_011543596.1:c.43_46delinsCAGG	XP_011541898.1:p.Gln15=
XM_011543597.1:c.43_46delinsCAGG	XP_011541899.1:p.Gln15=
XM_011543598.1:c.43_46delinsCAGG	XP_011541900.1:p.Gln15=
XM_011543598.3:c.43_46delinsCAGG	XP_011541900.1:p.Gln15=
XM_017009786.1:c.43_46delinsCAGG	XP_016865275.1:p.Gln15=
NM_000344.4:c.43_46delinsCAGG MANE Select	NP_000335.1:p.Gln15=