Canonical Allele Identifier: CA2276011943

Gene: AANAT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76469716C= , CM000679.2:g.76469716C=	GRCh38
NC_000017.10:g.74465798C= , CM000679.1:g.74465798C=	GRCh37
NC_000017.9:g.71977393C=	NCBI36
NG_015976.1:g.21366C=
NG_032852.1:g.36712G= , LRG_532:g.36712G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392492.8:c.370C= MANE Select	ENSP00000376282.2:p.Leu124=
ENST00000250615.7:c.505C=	ENSP00000250615.2:p.Leu169=
ENST00000392492.7:c.370C=	ENSP00000376282.2:p.Leu124=
ENST00000587798.1:c.*147C=	ENSP00000468239.1:n.*147C=
NM_001088.2:c.370C=	NP_001079.1:p.Leu124=
NM_001166579.1:c.505C=	NP_001160051.1:p.Leu169=
NR_110548.1:n.681C=
XM_011524415.1:c.370C=	XP_011522717.1:p.Leu124=
XM_011524416.1:c.577C=	XP_011522718.1:p.Leu193=
XM_011524417.1:c.577C=	XP_011522719.1:p.Leu193=
XM_011524418.1:c.577C=	XP_011522720.1:p.Leu193=
XM_011524419.1:c.577C=	XP_011522721.1:p.Leu193=
XM_011524420.1:c.577C=	XP_011522722.1:p.Leu193=
XM_011524421.1:c.577C=	XP_011522723.1:p.Leu193=
XM_011524422.1:c.460C=	XP_011522724.1:p.Leu154=
XM_011524423.1:c.370C=	XP_011522725.1:p.Leu124=
XM_017024259.1:c.484C=	XP_016879748.1:p.Leu162=
NM_001088.3:c.370C= MANE Select	NP_001079.1:p.Leu124=
NR_110548.2:n.626C=
NM_001166579.2:c.505C=	NP_001160051.1:p.Leu169=