Canonical Allele Identifier: CA444901707

Gene: SMN2

Linked Data

• MyVariant Identifiers: chr5:g.69372354A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.70076527A>C , CM000667.2:g.70076527A>C	GRCh38
NC_000005.9:g.69372354A>C , CM000667.1:g.69372354A>C	GRCh37
NC_000005.8:g.69408110A>C	NCBI36
NG_008728.1:g.32005A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380743.9:c.841A>C MANE Select	ENSP00000370119.4:p.Arg281=
ENST00000380741.8:c.841A>C	ENSP00000370117.5:p.Arg281=
ENST00000380742.8:c.745A>C	ENSP00000370118.4:p.Arg249=
ENST00000380743.8:c.841A>C	ENSP00000370119.4:p.Arg281=
ENST00000505346.5:n.307A>C
ENST00000506734.5:c.*59-492A>C	ENSP00000424799.1:n.*59-492A>C
ENST00000507458.2:c.95A>C
ENST00000511812.5:c.640A>C	ENSP00000424282.1:p.Arg214=
ENST00000514914.1:n.382A>C
ENST00000614240.4:c.745A>C	ENSP00000479279.1:p.Arg249=
ENST00000626847.2:c.835-492A>C	ENSP00000486152.1:n.835-492A>C
NM_017411.3:c.841A>C	NP_059107.1:p.Arg281=
NM_022875.2:c.835-492A>C	NP_075013.1:n.835-492A>C
NM_022876.2:c.745A>C	NP_075014.1:p.Arg249=
NM_022877.2:c.739-492A>C	NP_075015.1:n.739-492A>C
XM_011543600.1:c.640A>C	XP_011541902.1:p.Arg214=
XM_011543601.1:c.634-492A>C	XP_011541903.1:n.634-492A>C
XM_011543602.1:c.544A>C	XP_011541904.1:p.Arg182=
XM_011543603.1:c.538-492A>C	XP_011541905.1:n.538-492A>C
XR_948432.1:n.1054+88523A>C
XM_011543600.2:c.640A>C	XP_011541902.1:p.Arg214=
XM_011543602.3:c.544A>C	XP_011541904.1:p.Arg182=
XM_011543603.3:c.538-492A>C	XP_011541905.1:n.538-492A>C
NM_017411.4:c.841A>C MANE Select	NP_059107.1:p.Arg281=
NM_022875.3:c.835-492A>C	NP_075013.1:n.835-492A>C