Canonical Allele Identifier: CA2276011903

Gene: AANAT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76469643C= , CM000679.2:g.76469643C=	GRCh38
NC_000017.10:g.74465725C= , CM000679.1:g.74465725C=	GRCh37
NC_000017.9:g.71977320C=	NCBI36
NG_015976.1:g.21293C=
NG_032852.1:g.36785G= , LRG_532:g.36785G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000392492.8:c.319-22C= MANE Select	ENSP00000376282.2:n.319-22C=
ENST00000250615.7:c.454-22C=	ENSP00000250615.2:n.454-22C=
ENST00000392492.7:c.319-22C=	ENSP00000376282.2:n.319-22C=
ENST00000585649.1:c.433-22C=	ENSP00000468717.1:n.433-22C=
ENST00000587798.1:c.*96-22C=	ENSP00000468239.1:n.*96-22C=
NM_001088.2:c.319-22C=	NP_001079.1:n.319-22C=
NM_001166579.1:c.454-22C=	NP_001160051.1:n.454-22C=
NR_110548.1:n.630-22C=
XM_011524415.1:c.319-22C=	XP_011522717.1:n.319-22C=
XM_011524416.1:c.526-22C=	XP_011522718.1:n.526-22C=
XM_011524417.1:c.526-22C=	XP_011522719.1:n.526-22C=
XM_011524418.1:c.526-22C=	XP_011522720.1:n.526-22C=
XM_011524419.1:c.526-22C=	XP_011522721.1:n.526-22C=
XM_011524420.1:c.526-22C=	XP_011522722.1:n.526-22C=
XM_011524421.1:c.526-22C=	XP_011522723.1:n.526-22C=
XM_011524422.1:c.409-22C=	XP_011522724.1:n.409-22C=
XM_011524423.1:c.319-22C=	XP_011522725.1:n.319-22C=
XM_017024259.1:c.433-22C=	XP_016879748.1:n.433-22C=
NM_001088.3:c.319-22C= MANE Select	NP_001079.1:n.319-22C=
NR_110548.2:n.575-22C=
NM_001166579.2:c.454-22C=	NP_001160051.1:n.454-22C=