Canonical Allele Identifier: CA2550228421
Gene: AANAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.76469269dup , CM000679.2:g.76469269dup GRCh38
NC_000017.10:g.74465351dup , CM000679.1:g.74465351dup GRCh37
NC_000017.9:g.71976946dup NCBI36
NG_015976.1:g.20919dup
NG_032852.1:g.37159dup , LRG_532:g.37159dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000392492.8:c.260dup MANE Select ENSP00000376282.2:p.Cys89LeufsTer?
ENST00000250615.7:c.395dup ENSP00000250615.2:p.Cys134LeufsTer?
ENST00000392492.7:c.260dup ENSP00000376282.2:p.Cys89LeufsTer?
ENST00000585649.1:c.374dup ENSP00000468717.1:p.Cys127LeufsTer?
ENST00000587798.1:c.*37dup ENSP00000468239.1:n.*37dup
NM_001088.2:c.260dup NP_001079.1:p.Cys89LeufsTer?
NM_001166579.1:c.395dup NP_001160051.1:p.Cys134LeufsTer?
NR_110548.1:n.571dup
XM_011524415.1:c.260dup XP_011522717.1:p.Cys89LeufsTer?
XM_011524416.1:c.467dup XP_011522718.1:p.Cys158LeufsTer?
XM_011524417.1:c.467dup XP_011522719.1:p.Cys158LeufsTer?
XM_011524418.1:c.467dup XP_011522720.1:p.Cys158LeufsTer?
XM_011524419.1:c.467dup XP_011522721.1:p.Cys158LeufsTer?
XM_011524420.1:c.467dup XP_011522722.1:p.Cys158LeufsTer?
XM_011524421.1:c.467dup XP_011522723.1:p.Cys158LeufsTer?
XM_011524422.1:c.350dup XP_011522724.1:p.Cys119LeufsTer?
XM_011524423.1:c.260dup XP_011522725.1:p.Cys89LeufsTer?
XM_017024259.1:c.374dup XP_016879748.1:p.Cys127LeufsTer?
NM_001088.3:c.260dup MANE Select NP_001079.1:p.Cys89LeufsTer?
NR_110548.2:n.516dup
NM_001166579.2:c.395dup NP_001160051.1:p.Cys134LeufsTer?