Canonical Allele Identifier: CA360096735

Gene: SMN1

Linked Data

• MyVariant Identifiers: chr5:g.70241924A>C (hg19) ; chr5:g.70946097A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.70946097A>C , CM000667.2:g.70946097A>C	GRCh38
NC_000005.9:g.70241924A>C , CM000667.1:g.70241924A>C	GRCh37
NC_000005.8:g.70277680A>C	NCBI36
NG_008691.1:g.26157A>C , LRG_676:g.26157A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380707.9:c.755A>C MANE Select	ENSP00000370083.4:p.Asp252Ala
ENST00000351205.8:c.755A>C	ENSP00000305857.5:p.Asp252Ala
ENST00000380707.8:c.755A>C	ENSP00000370083.4:p.Asp252Ala
ENST00000503079.6:c.659A>C	ENSP00000428128.1:p.Asp220Ala
ENST00000506163.5:c.755A>C	ENSP00000424926.1:p.Asp252Ala
ENST00000506239.6:c.755A>C	ENSP00000422679.2:p.Asp252Ala
ENST00000510679.1:n.9A>C
ENST00000513228.1:n.322A>C
ENST00000514951.5:c.554A>C	ENSP00000423298.1:p.Asp185Ala
ENST00000518504.5:n.272A>C
ENST00000625245.2:c.755A>C	ENSP00000486539.1:p.Asp252Ala
NM_000344.3:c.755A>C , LRG_676t1:c.755A>C	NP_000335.1:p.Asp252Ala
NM_001297715.1:c.755A>C	NP_001284644.1:p.Asp252Ala
NM_022874.2:c.659A>C	NP_075012.1:p.Asp220Ala
XM_011543596.1:c.755A>C	XP_011541898.1:p.Asp252Ala
XM_011543597.1:c.554A>C	XP_011541899.1:p.Asp185Ala
XM_011543598.1:c.458A>C	XP_011541900.1:p.Asp153Ala
XM_011543598.3:c.458A>C	XP_011541900.1:p.Asp153Ala
XM_017009786.1:c.659A>C	XP_016865275.1:p.Asp220Ala
NM_000344.4:c.755A>C MANE Select	NP_000335.1:p.Asp252Ala