Canonical Allele Identifier: CA2276011956
Gene: AANAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.76469737C= , CM000679.2:g.76469737C= GRCh38
NC_000017.10:g.74465819C= , CM000679.1:g.74465819C= GRCh37
NC_000017.9:g.71977414C= NCBI36
NG_015976.1:g.21387C=
NG_032852.1:g.36691G= , LRG_532:g.36691G=

Transcript Alleles

HGVS Amino-acid change
ENST00000392492.8:c.391C= MANE Select ENSP00000376282.2:p.Arg131=
ENST00000250615.7:c.526C= ENSP00000250615.2:p.Arg176=
ENST00000392492.7:c.391C= ENSP00000376282.2:p.Arg131=
ENST00000587798.1:c.*168C= ENSP00000468239.1:n.*168C=
NM_001088.2:c.391C= NP_001079.1:p.Arg131=
NM_001166579.1:c.526C= NP_001160051.1:p.Arg176=
NR_110548.1:n.702C=
XM_011524415.1:c.391C= XP_011522717.1:p.Arg131=
XM_011524416.1:c.598C= XP_011522718.1:p.Arg200=
XM_011524417.1:c.598C= XP_011522719.1:p.Arg200=
XM_011524418.1:c.598C= XP_011522720.1:p.Arg200=
XM_011524419.1:c.598C= XP_011522721.1:p.Arg200=
XM_011524420.1:c.598C= XP_011522722.1:p.Arg200=
XM_011524421.1:c.598C= XP_011522723.1:p.Arg200=
XM_011524422.1:c.481C= XP_011522724.1:p.Arg161=
XM_011524423.1:c.391C= XP_011522725.1:p.Arg131=
XM_017024259.1:c.505C= XP_016879748.1:p.Arg169=
NM_001088.3:c.391C= MANE Select NP_001079.1:p.Arg131=
NR_110548.2:n.647C=
NM_001166579.2:c.526C= NP_001160051.1:p.Arg176=