Canonical Allele Identifier: CA2229530531

Gene: NUTF2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67868167G= , CM000678.2:g.67868167G=	GRCh38
NC_000016.9:g.67902070G= , CM000678.1:g.67902070G=	GRCh37
NC_000016.8:g.66459571G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_005796.3:c.100-173G= MANE Select	NP_005787.1:n.100-173G=
ENST00000219169.9:c.100-173G= MANE Select	ENSP00000219169.4:n.100-173G=
NM_001322038.1:c.100-173G=	NP_001308967.1:n.100-173G=
NM_001322038.2:c.100-173G=	NP_001308967.1:n.100-173G=
NM_001322039.1:c.100-173G=	NP_001308968.1:n.100-173G=
NM_001322039.2:c.100-173G=	NP_001308968.1:n.100-173G=
NM_001322040.1:c.100-173G=	NP_001308969.1:n.100-173G=
NM_001322040.2:c.100-173G=	NP_001308969.1:n.100-173G=
NM_001322041.1:c.100-173G=	NP_001308970.1:n.100-173G=
NM_001322041.2:c.100-173G=	NP_001308970.1:n.100-173G=
NM_005796.1:c.100-173G=	NP_005787.1:n.100-173G=
NM_005796.2:c.100-173G=	NP_005787.1:n.100-173G=
ENST00000219169.8:c.100-173G=	ENSP00000219169.4:n.100-173G=
ENST00000567105.5:c.100-173G=	ENSP00000456428.1:n.100-173G=
ENST00000568233.5:n.180-173G=
ENST00000568233.6:c.100-173G=	ENSP00000515099.1:n.100-173G=
ENST00000568390.5:n.192-173G=
ENST00000568396.2:c.100-173G=	ENSP00000457022.1:n.100-173G=
ENST00000569436.6:c.100-173G=	ENSP00000457989.1:n.100-173G=
ENST00000569436.7:c.100-173G=	ENSP00000457989.1:n.100-173G=
ENST00000570026.1:n.244-173G=
ENST00000570026.2:c.100-173G=	ENSP00000515106.1:n.100-173G=
ENST00000700610.1:c.100-173G=	ENSP00000515098.1:n.100-173G=
ENST00000700611.1:c.-150-173G=	ENSP00000515101.1:n.-150-173G=
ENST00000700612.1:c.100-173G=	ENSP00000515102.1:n.100-173G=
ENST00000700613.1:c.100-173G=	ENSP00000515103.1:n.100-173G=
ENST00000700614.1:c.100-173G=	ENSP00000515104.1:n.100-173G=
ENST00000700615.1:c.-150-173G=	ENSP00000515105.1:n.-150-173G=
XM_005255771.1:c.100-173G=	XP_005255828.1:n.100-173G=