Canonical Allele Identifier: CA1539745088

Gene: NUP155

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37341164C= , CM000667.2:g.37341164C=	GRCh38
NC_000005.9:g.37341266C= , CM000667.1:g.37341266C=	GRCh37
NC_000005.8:g.37377023C=	NCBI36
NG_034131.1:g.34963G=

Transcript Alleles

HGVS	Amino-acid Change
NM_153485.3:c.1172G= MANE Select	NP_705618.1:p.Arg391=
ENST00000231498.8:c.1172G= MANE Select	ENSP00000231498.3:p.Arg391=
NM_001278312.1:c.1172G=	NP_001265241.1:p.Arg391=
NM_001278312.2:c.1172G=	NP_001265241.1:p.Arg391=
NM_004298.3:c.995G=	NP_004289.1:p.Arg332=
NM_004298.4:c.995G=	NP_004289.1:p.Arg332=
NM_153485.2:c.1172G=	NP_705618.1:p.Arg391=
ENST00000231498.7:c.1172G=	ENSP00000231498.3:p.Arg391=
ENST00000381843.6:c.995G=	ENSP00000371265.2:p.Arg332=
ENST00000513532.1:c.1172G=	ENSP00000422019.1:p.Arg391=
XM_011514164.1:c.1172G=	XP_011512466.1:p.Arg391=
XM_011514165.1:c.1172G=	XP_011512467.1:p.Arg391=
XM_011514165.3:c.1172G=	XP_011512467.1:p.Arg391=
XM_011514166.1:c.1172G=	XP_011512468.1:p.Arg391=
XR_001742368.2:n.1290G=
XR_001742369.2:n.1290G=