Canonical Allele Identifier: CA2276011960
Gene: AANAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.76469742G= , CM000679.2:g.76469742G= GRCh38
NC_000017.10:g.74465824G= , CM000679.1:g.74465824G= GRCh37
NC_000017.9:g.71977419G= NCBI36
NG_015976.1:g.21392G=
NG_032852.1:g.36686C= , LRG_532:g.36686C=

Transcript Alleles

HGVS Amino-acid change
ENST00000392492.8:c.396G= MANE Select ENSP00000376282.2:p.Gln132=
ENST00000250615.7:c.531G= ENSP00000250615.2:p.Gln177=
ENST00000392492.7:c.396G= ENSP00000376282.2:p.Gln132=
ENST00000587798.1:c.*173G= ENSP00000468239.1:n.*173G=
NM_001088.2:c.396G= NP_001079.1:p.Gln132=
NM_001166579.1:c.531G= NP_001160051.1:p.Gln177=
NR_110548.1:n.707G=
XM_011524415.1:c.396G= XP_011522717.1:p.Gln132=
XM_011524416.1:c.603G= XP_011522718.1:p.Gln201=
XM_011524417.1:c.603G= XP_011522719.1:p.Gln201=
XM_011524418.1:c.603G= XP_011522720.1:p.Gln201=
XM_011524419.1:c.603G= XP_011522721.1:p.Gln201=
XM_011524420.1:c.603G= XP_011522722.1:p.Gln201=
XM_011524421.1:c.603G= XP_011522723.1:p.Gln201=
XM_011524422.1:c.486G= XP_011522724.1:p.Gln162=
XM_011524423.1:c.396G= XP_011522725.1:p.Gln132=
XM_017024259.1:c.510G= XP_016879748.1:p.Gln170=
NM_001088.3:c.396G= MANE Select NP_001079.1:p.Gln132=
NR_110548.2:n.652G=
NM_001166579.2:c.531G= NP_001160051.1:p.Gln177=