Canonical Allele Identifier: CA2337640550

Gene: SMG9

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43744768T= , CM000681.2:g.43744768T=	GRCh38
NC_000019.9:g.44248920T= , CM000681.1:g.44248920T=	GRCh37
NC_000019.8:g.48940760T=	NCBI36
NG_051200.1:g.15269A=

Transcript Alleles

HGVS	Amino-acid Change
NM_019108.4:c.701+4A= MANE Select	NP_061981.2:n.701+4A=
ENST00000270066.11:c.701+4A= MANE Select	ENSP00000270066.6:n.701+4A=
NM_019108.2:c.701+4A=	NP_061981.2:n.701+4A=
NM_019108.3:c.701+4A=	NP_061981.2:n.701+4A=
ENST00000270066.10:c.701+4A=	ENSP00000270066.6:n.701+4A=
ENST00000595700.5:n.921+4A=
ENST00000597598.1:c.313+4A=
ENST00000601170.5:c.701+4A=	ENSP00000471398.1:n.701+4A=
XM_005259057.2:c.701+4A=	XP_005259114.1:n.701+4A=
XM_005259057.3:c.701+4A=	XP_005259114.1:n.701+4A=
XM_011527113.1:c.701+4A=	XP_011525415.1:n.701+4A=
XM_011527114.1:c.701+4A=	XP_011525416.1:n.701+4A=
XM_011527115.1:c.701+4A=	XP_011525417.1:n.701+4A=
XM_011527116.1:c.701+4A=	XP_011525418.1:n.701+4A=
XM_011527117.1:c.-32+2674A=	XP_011525419.1:n.-32+2674A=
XM_017026988.1:c.-32+2674A=	XP_016882477.1:n.-32+2674A=
XM_024451608.1:c.-32+2674A=	XP_024307376.1:n.-32+2674A=