Canonical Allele Identifier: CA1554041000

Gene: SMN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.70049647A= , CM000667.2:g.70049647A=	GRCh38
NC_000005.9:g.69345474A= , CM000667.1:g.69345474A=	GRCh37
NC_000005.8:g.69381230A=	NCBI36
NG_008728.1:g.5125A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380743.8:c.-39A=	ENSP00000370119.4:n.-39A=
ENST00000511812.5:c.-39A=	ENSP00000424282.1:n.-39A=
NM_017411.3:c.-39A=	NP_059107.1:n.-39A=
NM_022875.2:c.-39A=	NP_075013.1:n.-39A=
NM_022876.2:c.-39A=	NP_075014.1:n.-39A=
NM_022877.2:c.-39A=	NP_075015.1:n.-39A=
XM_011543599.1:c.-39A=	XP_011541901.1:n.-39A=
XM_011543600.1:c.-39A=	XP_011541902.1:n.-39A=
XM_011543601.1:c.-39A=	XP_011541903.1:n.-39A=
XM_011543602.1:c.-39A=	XP_011541904.1:n.-39A=
XM_011543603.1:c.-39A=	XP_011541905.1:n.-39A=
XR_948432.1:n.1054+61643A=
XM_011543600.2:c.-39A=	XP_011541902.1:n.-39A=
XM_011543602.3:c.-39A=	XP_011541904.1:n.-39A=
XM_011543603.3:c.-39A=	XP_011541905.1:n.-39A=
XM_017009787.1:c.-39A=	XP_016865276.1:n.-39A=