Canonical Allele Identifier: CA2276010979

Gene: AANAT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76467680G= , CM000679.2:g.76467680G=	GRCh38
NC_000017.10:g.74463762G= , CM000679.1:g.74463762G=	GRCh37
NC_000017.9:g.71975357G=	NCBI36
NG_015976.1:g.19330G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392492.8:c.-123G= MANE Select	ENSP00000376282.2:n.-123G=
ENST00000250615.7:c.61-992G=	ENSP00000250615.2:n.61-992G=
ENST00000392492.7:c.-123G=	ENSP00000376282.2:n.-123G=
NM_001088.2:c.-123G=	NP_001079.1:n.-123G=
NM_001166579.1:c.61-992G=	NP_001160051.1:n.61-992G=
NR_110548.1:n.133G=
XM_011524415.1:c.-75-992G=	XP_011522717.1:n.-75-992G=
XM_011524416.1:c.133-992G=	XP_011522718.1:n.133-992G=
XM_011524417.1:c.133-992G=	XP_011522719.1:n.133-992G=
XM_011524418.1:c.133-992G=	XP_011522720.1:n.133-992G=
XM_011524419.1:c.133-992G=	XP_011522721.1:n.133-992G=
XM_011524420.1:c.133-992G=	XP_011522722.1:n.133-992G=
XM_011524421.1:c.133-992G=	XP_011522723.1:n.133-992G=
XM_011524422.1:c.16-992G=	XP_011522724.1:n.16-992G=
XM_011524423.1:c.-75-992G=	XP_011522725.1:n.-75-992G=
XM_017024259.1:c.-953G=	XP_016879748.1:n.-953G=
NM_001088.3:c.-123G= MANE Select	NP_001079.1:n.-123G=
NR_110548.2:n.78G=
NM_001166579.2:c.61-992G=	NP_001160051.1:n.61-992G=