Canonical Allele Identifier: CA360086954

Gene: SMN2

Linked Data

• MyVariant Identifiers: chr5:g.69372355G>C (hg19) ; chr5:g.70076528G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.70076528G>C , CM000667.2:g.70076528G>C	GRCh38
NC_000005.9:g.69372355G>C , CM000667.1:g.69372355G>C	GRCh37
NC_000005.8:g.69408111G>C	NCBI36
NG_008728.1:g.32006G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380743.9:c.842G>C MANE Select	ENSP00000370119.4:p.Arg281Thr
ENST00000380741.8:c.842G>C	ENSP00000370117.5:p.Arg281Thr
ENST00000380742.8:c.746G>C	ENSP00000370118.4:p.Arg249Thr
ENST00000380743.8:c.842G>C	ENSP00000370119.4:p.Arg281Thr
ENST00000505346.5:n.308G>C
ENST00000506734.5:c.*59-491G>C	ENSP00000424799.1:n.*59-491G>C
ENST00000507458.2:c.96G>C
ENST00000511812.5:c.641G>C	ENSP00000424282.1:p.Arg214Thr
ENST00000514914.1:n.383G>C
ENST00000614240.4:c.746G>C	ENSP00000479279.1:p.Arg249Thr
ENST00000626847.2:c.835-491G>C	ENSP00000486152.1:n.835-491G>C
NM_017411.3:c.842G>C	NP_059107.1:p.Arg281Thr
NM_022875.2:c.835-491G>C	NP_075013.1:n.835-491G>C
NM_022876.2:c.746G>C	NP_075014.1:p.Arg249Thr
NM_022877.2:c.739-491G>C	NP_075015.1:n.739-491G>C
XM_011543600.1:c.641G>C	XP_011541902.1:p.Arg214Thr
XM_011543601.1:c.634-491G>C	XP_011541903.1:n.634-491G>C
XM_011543602.1:c.545G>C	XP_011541904.1:p.Arg182Thr
XM_011543603.1:c.538-491G>C	XP_011541905.1:n.538-491G>C
XR_948432.1:n.1054+88524G>C
XM_011543600.2:c.641G>C	XP_011541902.1:p.Arg214Thr
XM_011543602.3:c.545G>C	XP_011541904.1:p.Arg182Thr
XM_011543603.3:c.538-491G>C	XP_011541905.1:n.538-491G>C
NM_017411.4:c.842G>C MANE Select	NP_059107.1:p.Arg281Thr
NM_022875.3:c.835-491G>C	NP_075013.1:n.835-491G>C