Canonical Allele Identifier: CA2258188317

Gene: AATF

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.36949012G= , CM000679.2:g.36949012G=	GRCh38
NC_000017.10:g.35306312G= , CM000679.1:g.35306312G=	GRCh37
NC_000017.9:g.32380425G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_012138.4:c.-114G= MANE Select	NP_036270.1:n.-114G=
ENST00000619387.5:c.-114G= MANE Select	ENSP00000477848.1:n.-114G=
NM_012138.3:c.-114G=	NP_036270.1:n.-114G=
ENST00000616434.2:c.-114G=	ENSP00000477881.2:n.-114G=
ENST00000619387.4:c.-114G=	ENSP00000477848.1:n.-114G=
ENST00000679508.1:n.88G=
ENST00000679985.1:n.88G=
ENST00000679997.1:c.-114G=	ENSP00000505070.1:n.-114G=
ENST00000680330.1:c.-114G=	ENSP00000506539.1:n.-114G=
ENST00000680340.1:c.-114G=	ENSP00000506264.1:n.-114G=
ENST00000680356.1:c.-114G=	ENSP00000505146.1:n.-114G=
ENST00000680579.1:c.-114G=	ENSP00000506655.1:n.-114G=
ENST00000680807.1:n.88G=
ENST00000681070.1:n.46G=
ENST00000681800.1:n.88G=
XM_011524611.1:c.-114G=	XP_011522913.1:n.-114G=
XM_011524611.2:c.-114G=	XP_011522913.1:n.-114G=
XR_934439.1:n.122G=
XR_934439.3:n.59G=