Canonical Allele Identifier: CA1554042390

Gene: SMN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.70070929T= , CM000667.2:g.70070929T=	GRCh38
NC_000005.9:g.69366756T= , CM000667.1:g.69366756T=	GRCh37
NC_000005.8:g.69402512T=	NCBI36
NG_008728.1:g.26407T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380743.9:c.834+178T= MANE Select	ENSP00000370119.4:n.834+178T=
ENST00000638794.1:c.834+178T=	ENSP00000492675.1:n.834+178T=
ENST00000380741.8:c.834+178T=	ENSP00000370117.5:n.834+178T=
ENST00000380742.8:c.738+178T=	ENSP00000370118.4:n.738+178T=
ENST00000380743.8:c.834+178T=	ENSP00000370119.4:n.834+178T=
ENST00000505346.5:n.300+178T=
ENST00000506734.5:c.834+178T=	ENSP00000424799.1:n.834+178T=
ENST00000507458.2:c.88+178T=
ENST00000511812.5:c.633+178T=	ENSP00000424282.1:n.633+178T=
ENST00000514914.1:n.375+178T=
ENST00000614240.4:c.738+178T=	ENSP00000479279.1:n.738+178T=
ENST00000626847.2:c.834+178T=	ENSP00000486152.1:n.834+178T=
ENST00000628696.2:c.834+178T=	ENSP00000486268.1:n.834+178T=
NM_017411.3:c.834+178T=	NP_059107.1:n.834+178T=
NM_022875.2:c.834+178T=	NP_075013.1:n.834+178T=
NM_022876.2:c.738+178T=	NP_075014.1:n.738+178T=
NM_022877.2:c.738+178T=	NP_075015.1:n.738+178T=
XM_011543599.1:c.834+178T=	XP_011541901.1:n.834+178T=
XM_011543600.1:c.633+178T=	XP_011541902.1:n.633+178T=
XM_011543601.1:c.633+178T=	XP_011541903.1:n.633+178T=
XM_011543602.1:c.537+178T=	XP_011541904.1:n.537+178T=
XM_011543603.1:c.537+178T=	XP_011541905.1:n.537+178T=
XR_948432.1:n.1054+82925T=
XM_011543600.2:c.633+178T=	XP_011541902.1:n.633+178T=
XM_011543602.3:c.537+178T=	XP_011541904.1:n.537+178T=
XM_011543603.3:c.537+178T=	XP_011541905.1:n.537+178T=
XM_017009787.1:c.834+178T=	XP_016865276.1:n.834+178T=
NM_017411.4:c.834+178T= MANE Select	NP_059107.1:n.834+178T=
NM_022875.3:c.834+178T=	NP_075013.1:n.834+178T=