Canonical Allele Identifier: CA2276011711

Gene: AANAT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76469272G= , CM000679.2:g.76469272G=	GRCh38
NC_000017.10:g.74465354G= , CM000679.1:g.74465354G=	GRCh37
NC_000017.9:g.71976949G=	NCBI36
NG_015976.1:g.20922G=
NG_032852.1:g.37156C= , LRG_532:g.37156C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392492.8:c.263G= MANE Select	ENSP00000376282.2:p.Gly88=
ENST00000250615.7:c.398G=	ENSP00000250615.2:p.Gly133=
ENST00000392492.7:c.263G=	ENSP00000376282.2:p.Gly88=
ENST00000585649.1:c.377G=	ENSP00000468717.1:p.Gly126=
ENST00000587798.1:c.*40G=	ENSP00000468239.1:n.*40G=
NM_001088.2:c.263G=	NP_001079.1:p.Gly88=
NM_001166579.1:c.398G=	NP_001160051.1:p.Gly133=
NR_110548.1:n.574G=
XM_011524415.1:c.263G=	XP_011522717.1:p.Gly88=
XM_011524416.1:c.470G=	XP_011522718.1:p.Gly157=
XM_011524417.1:c.470G=	XP_011522719.1:p.Gly157=
XM_011524418.1:c.470G=	XP_011522720.1:p.Gly157=
XM_011524419.1:c.470G=	XP_011522721.1:p.Gly157=
XM_011524420.1:c.470G=	XP_011522722.1:p.Gly157=
XM_011524421.1:c.470G=	XP_011522723.1:p.Gly157=
XM_011524422.1:c.353G=	XP_011522724.1:p.Gly118=
XM_011524423.1:c.263G=	XP_011522725.1:p.Gly88=
XM_017024259.1:c.377G=	XP_016879748.1:p.Gly126=
NM_001088.3:c.263G= MANE Select	NP_001079.1:p.Gly88=
NR_110548.2:n.519G=
NM_001166579.2:c.398G=	NP_001160051.1:p.Gly133=