Canonical Allele Identifier: CA2276011727

Gene: AANAT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76469307G= , CM000679.2:g.76469307G=	GRCh38
NC_000017.10:g.74465389G= , CM000679.1:g.74465389G=	GRCh37
NC_000017.9:g.71976984G=	NCBI36
NG_015976.1:g.20957G=
NG_032852.1:g.37121C= , LRG_532:g.37121C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392492.8:c.298G= MANE Select	ENSP00000376282.2:p.Asp100=
ENST00000250615.7:c.433G=	ENSP00000250615.2:p.Asp145=
ENST00000392492.7:c.298G=	ENSP00000376282.2:p.Asp100=
ENST00000585649.1:c.412G=	ENSP00000468717.1:p.Asp138=
ENST00000587798.1:c.*75G=	ENSP00000468239.1:n.*75G=
NM_001088.2:c.298G=	NP_001079.1:p.Asp100=
NM_001166579.1:c.433G=	NP_001160051.1:p.Asp145=
NR_110548.1:n.609G=
XM_011524415.1:c.298G=	XP_011522717.1:p.Asp100=
XM_011524416.1:c.505G=	XP_011522718.1:p.Asp169=
XM_011524417.1:c.505G=	XP_011522719.1:p.Asp169=
XM_011524418.1:c.505G=	XP_011522720.1:p.Asp169=
XM_011524419.1:c.505G=	XP_011522721.1:p.Asp169=
XM_011524420.1:c.505G=	XP_011522722.1:p.Asp169=
XM_011524421.1:c.505G=	XP_011522723.1:p.Asp169=
XM_011524422.1:c.388G=	XP_011522724.1:p.Asp130=
XM_011524423.1:c.298G=	XP_011522725.1:p.Asp100=
XM_017024259.1:c.412G=	XP_016879748.1:p.Asp138=
NM_001088.3:c.298G= MANE Select	NP_001079.1:p.Asp100=
NR_110548.2:n.554G=
NM_001166579.2:c.433G=	NP_001160051.1:p.Asp145=