Canonical Allele Identifier: CA2576448786
Gene: AANAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.76467696del , CM000679.2:g.76467696del GRCh38
NC_000017.10:g.74463778del , CM000679.1:g.74463778del GRCh37
NC_000017.9:g.71975373del NCBI36
NG_015976.1:g.19346del

Transcript Alleles

HGVS Amino-acid Change
ENST00000392492.8:c.-107del MANE Select ENSP00000376282.2:n.-107del
ENST00000250615.7:c.61-976del ENSP00000250615.2:n.61-976del
ENST00000392492.7:c.-107del ENSP00000376282.2:n.-107del
NM_001088.2:c.-107del NP_001079.1:n.-107del
NM_001166579.1:c.61-976del NP_001160051.1:n.61-976del
NR_110548.1:n.149del
XM_011524415.1:c.-75-976del XP_011522717.1:n.-75-976del
XM_011524416.1:c.133-976del XP_011522718.1:n.133-976del
XM_011524417.1:c.133-976del XP_011522719.1:n.133-976del
XM_011524418.1:c.133-976del XP_011522720.1:n.133-976del
XM_011524419.1:c.133-976del XP_011522721.1:n.133-976del
XM_011524420.1:c.133-976del XP_011522722.1:n.133-976del
XM_011524421.1:c.133-976del XP_011522723.1:n.133-976del
XM_011524422.1:c.16-976del XP_011522724.1:n.16-976del
XM_011524423.1:c.-75-976del XP_011522725.1:n.-75-976del
XM_017024259.1:c.-937del XP_016879748.1:n.-937del
NM_001088.3:c.-107del MANE Select NP_001079.1:n.-107del
NR_110548.2:n.94del
NM_001166579.2:c.61-976del NP_001160051.1:n.61-976del