Canonical Allele Identifier: CA2639993318
Gene: AANAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.76467560_76467564del , CM000679.2:g.76467560_76467564del GRCh38
NC_000017.10:g.74463642_74463646del , CM000679.1:g.74463642_74463646del GRCh37
NC_000017.9:g.71975237_71975241del NCBI36
NG_015976.1:g.19210_19214del

Transcript Alleles

HGVS Amino-acid Change
ENST00000250615.7:c.61-1112_61-1108del ENSP00000250615.2:n.61-1112_61-1108del
NM_001088.2:c.-243_-239del NP_001079.1:n.-243_-239del
NM_001166579.1:c.61-1112_61-1108del NP_001160051.1:n.61-1112_61-1108del
NR_110548.1:n.13_17del
XM_011524415.1:c.-75-1112_-75-1108del XP_011522717.1:n.-75-1112_-75-1108del
XM_011524416.1:c.133-1112_133-1108del XP_011522718.1:n.133-1112_133-1108del
XM_011524417.1:c.133-1112_133-1108del XP_011522719.1:n.133-1112_133-1108del
XM_011524418.1:c.133-1112_133-1108del XP_011522720.1:n.133-1112_133-1108del
XM_011524419.1:c.133-1112_133-1108del XP_011522721.1:n.133-1112_133-1108del
XM_011524420.1:c.133-1112_133-1108del XP_011522722.1:n.133-1112_133-1108del
XM_011524421.1:c.133-1112_133-1108del XP_011522723.1:n.133-1112_133-1108del
XM_011524422.1:c.16-1112_16-1108del XP_011522724.1:n.16-1112_16-1108del
XM_011524423.1:c.-75-1112_-75-1108del XP_011522725.1:n.-75-1112_-75-1108del
XM_017024259.1:c.-1073_-1069del XP_016879748.1:n.-1073_-1069del
NM_001166579.2:c.61-1112_61-1108del NP_001160051.1:n.61-1112_61-1108del