Canonical Allele Identifier: CA444901725

Gene: SMN2

Linked Data

• MyVariant Identifiers: chr5:g.69372390T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.70076563T>C , CM000667.2:g.70076563T>C	GRCh38
NC_000005.9:g.69372390T>C , CM000667.1:g.69372390T>C	GRCh37
NC_000005.8:g.69408146T>C	NCBI36
NG_008728.1:g.32041T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380743.9:c.877T>C MANE Select	ENSP00000370119.4:p.Leu293=
ENST00000380741.8:c.877T>C	ENSP00000370117.5:p.Leu293=
ENST00000380742.8:c.781T>C	ENSP00000370118.4:p.Leu261=
ENST00000380743.8:c.877T>C	ENSP00000370119.4:p.Leu293=
ENST00000505346.5:n.343T>C
ENST00000506734.5:c.*59-456T>C	ENSP00000424799.1:n.*59-456T>C
ENST00000507458.2:c.131T>C
ENST00000511812.5:c.676T>C	ENSP00000424282.1:p.Leu226=
ENST00000514914.1:n.418T>C
ENST00000614240.4:c.781T>C	ENSP00000479279.1:p.Leu261=
ENST00000626847.2:c.835-456T>C	ENSP00000486152.1:n.835-456T>C
NM_017411.3:c.877T>C	NP_059107.1:p.Leu293=
NM_022875.2:c.835-456T>C	NP_075013.1:n.835-456T>C
NM_022876.2:c.781T>C	NP_075014.1:p.Leu261=
NM_022877.2:c.739-456T>C	NP_075015.1:n.739-456T>C
XM_011543600.1:c.676T>C	XP_011541902.1:p.Leu226=
XM_011543601.1:c.634-456T>C	XP_011541903.1:n.634-456T>C
XM_011543602.1:c.580T>C	XP_011541904.1:p.Leu194=
XM_011543603.1:c.538-456T>C	XP_011541905.1:n.538-456T>C
XR_948432.1:n.1054+88559T>C
XM_011543600.2:c.676T>C	XP_011541902.1:p.Leu226=
XM_011543602.3:c.580T>C	XP_011541904.1:p.Leu194=
XM_011543603.3:c.538-456T>C	XP_011541905.1:n.538-456T>C
NM_017411.4:c.877T>C MANE Select	NP_059107.1:p.Leu293=
NM_022875.3:c.835-456T>C	NP_075013.1:n.835-456T>C