Canonical Allele Identifier: CA360086169

Gene: SMN2

Linked Data

• MyVariant Identifiers: chr5:g.69366477C>A (hg19) ; chr5:g.70070650C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.70070650C>A , CM000667.2:g.70070650C>A	GRCh38
NC_000005.9:g.69366477C>A , CM000667.1:g.69366477C>A	GRCh37
NC_000005.8:g.69402233C>A	NCBI36
NG_008728.1:g.26128C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000380743.9:c.733C>A MANE Select	ENSP00000370119.4:p.Pro245Thr
ENST00000638794.1:c.733C>A	ENSP00000492675.1:p.Pro245Thr
ENST00000380741.8:c.733C>A	ENSP00000370117.5:p.Pro245Thr
ENST00000380742.8:c.637C>A	ENSP00000370118.4:p.Pro213Thr
ENST00000380743.8:c.733C>A	ENSP00000370119.4:p.Pro245Thr
ENST00000503678.5:n.656C>A
ENST00000505346.5:n.199C>A
ENST00000506734.5:c.733C>A	ENSP00000424799.1:p.Pro245Thr
ENST00000508258.1:n.108C>A
ENST00000509805.5:n.300C>A
ENST00000511812.5:c.532C>A	ENSP00000424282.1:p.Pro178Thr
ENST00000511873.6:c.427C>A	ENSP00000475824.1:n.427C>A
ENST00000514914.1:n.274C>A
ENST00000614240.4:c.637C>A	ENSP00000479279.1:p.Pro213Thr
ENST00000626847.2:c.733C>A	ENSP00000486152.1:p.Pro245Thr
ENST00000628696.2:c.733C>A	ENSP00000486268.1:p.Pro245Thr
NM_017411.3:c.733C>A	NP_059107.1:p.Pro245Thr
NM_022875.2:c.733C>A	NP_075013.1:p.Pro245Thr
NM_022876.2:c.637C>A	NP_075014.1:p.Pro213Thr
NM_022877.2:c.637C>A	NP_075015.1:p.Pro213Thr
XM_011543599.1:c.733C>A	XP_011541901.1:p.Pro245Thr
XM_011543600.1:c.532C>A	XP_011541902.1:p.Pro178Thr
XM_011543601.1:c.532C>A	XP_011541903.1:p.Pro178Thr
XM_011543602.1:c.436C>A	XP_011541904.1:p.Pro146Thr
XM_011543603.1:c.436C>A	XP_011541905.1:p.Pro146Thr
XR_948432.1:n.1054+82646C>A
XM_011543600.2:c.532C>A	XP_011541902.1:p.Pro178Thr
XM_011543602.3:c.436C>A	XP_011541904.1:p.Pro146Thr
XM_011543603.3:c.436C>A	XP_011541905.1:p.Pro146Thr
XM_017009787.1:c.733C>A	XP_016865276.1:p.Pro245Thr
NM_017411.4:c.733C>A MANE Select	NP_059107.1:p.Pro245Thr
NM_022875.3:c.733C>A	NP_075013.1:p.Pro245Thr