Canonical Allele Identifier: CA360086513

Gene: SMN2

Linked Data

• MyVariant Identifiers: chr5:g.69366551G>C (hg19) ; chr5:g.70070724G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.70070724G>C , CM000667.2:g.70070724G>C	GRCh38
NC_000005.9:g.69366551G>C , CM000667.1:g.69366551G>C	GRCh37
NC_000005.8:g.69402307G>C	NCBI36
NG_008728.1:g.26202G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380743.9:c.807G>C MANE Select	ENSP00000370119.4:p.Met269Ile
ENST00000638794.1:c.807G>C	ENSP00000492675.1:p.Met269Ile
ENST00000380741.8:c.807G>C	ENSP00000370117.5:p.Met269Ile
ENST00000380742.8:c.711G>C	ENSP00000370118.4:p.Met237Ile
ENST00000380743.8:c.807G>C	ENSP00000370119.4:p.Met269Ile
ENST00000503678.5:n.730G>C
ENST00000505346.5:n.273G>C
ENST00000506734.5:c.807G>C	ENSP00000424799.1:p.Met269Ile
ENST00000507458.2:c.61G>C
ENST00000508258.1:n.182G>C
ENST00000509805.5:n.374G>C
ENST00000511812.5:c.606G>C	ENSP00000424282.1:p.Met202Ile
ENST00000514914.1:n.348G>C
ENST00000614240.4:c.711G>C	ENSP00000479279.1:p.Met237Ile
ENST00000626847.2:c.807G>C	ENSP00000486152.1:p.Met269Ile
ENST00000628696.2:c.807G>C	ENSP00000486268.1:p.Met269Ile
NM_017411.3:c.807G>C	NP_059107.1:p.Met269Ile
NM_022875.2:c.807G>C	NP_075013.1:p.Met269Ile
NM_022876.2:c.711G>C	NP_075014.1:p.Met237Ile
NM_022877.2:c.711G>C	NP_075015.1:p.Met237Ile
XM_011543599.1:c.807G>C	XP_011541901.1:p.Met269Ile
XM_011543600.1:c.606G>C	XP_011541902.1:p.Met202Ile
XM_011543601.1:c.606G>C	XP_011541903.1:p.Met202Ile
XM_011543602.1:c.510G>C	XP_011541904.1:p.Met170Ile
XM_011543603.1:c.510G>C	XP_011541905.1:p.Met170Ile
XR_948432.1:n.1054+82720G>C
XM_011543600.2:c.606G>C	XP_011541902.1:p.Met202Ile
XM_011543602.3:c.510G>C	XP_011541904.1:p.Met170Ile
XM_011543603.3:c.510G>C	XP_011541905.1:p.Met170Ile
XM_017009787.1:c.807G>C	XP_016865276.1:p.Met269Ile
NM_017411.4:c.807G>C MANE Select	NP_059107.1:p.Met269Ile
NM_022875.3:c.807G>C	NP_075013.1:p.Met269Ile