Canonical Allele Identifier: CA2276011719

Gene: AANAT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76469289A= , CM000679.2:g.76469289A=	GRCh38
NC_000017.10:g.74465371A= , CM000679.1:g.74465371A=	GRCh37
NC_000017.9:g.71976966A=	NCBI36
NG_015976.1:g.20939A=
NG_032852.1:g.37139T= , LRG_532:g.37139T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392492.8:c.280A= MANE Select	ENSP00000376282.2:p.Ile94=
ENST00000250615.7:c.415A=	ENSP00000250615.2:p.Ile139=
ENST00000392492.7:c.280A=	ENSP00000376282.2:p.Ile94=
ENST00000585649.1:c.394A=	ENSP00000468717.1:p.Ile132=
ENST00000587798.1:c.*57A=	ENSP00000468239.1:n.*57A=
NM_001088.2:c.280A=	NP_001079.1:p.Ile94=
NM_001166579.1:c.415A=	NP_001160051.1:p.Ile139=
NR_110548.1:n.591A=
XM_011524415.1:c.280A=	XP_011522717.1:p.Ile94=
XM_011524416.1:c.487A=	XP_011522718.1:p.Ile163=
XM_011524417.1:c.487A=	XP_011522719.1:p.Ile163=
XM_011524418.1:c.487A=	XP_011522720.1:p.Ile163=
XM_011524419.1:c.487A=	XP_011522721.1:p.Ile163=
XM_011524420.1:c.487A=	XP_011522722.1:p.Ile163=
XM_011524421.1:c.487A=	XP_011522723.1:p.Ile163=
XM_011524422.1:c.370A=	XP_011522724.1:p.Ile124=
XM_011524423.1:c.280A=	XP_011522725.1:p.Ile94=
XM_017024259.1:c.394A=	XP_016879748.1:p.Ile132=
NM_001088.3:c.280A= MANE Select	NP_001079.1:p.Ile94=
NR_110548.2:n.536A=
NM_001166579.2:c.415A=	NP_001160051.1:p.Ile139=