Canonical Allele Identifier: CA2276010981
Gene: AANAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.76467684G= , CM000679.2:g.76467684G= GRCh38
NC_000017.10:g.74463766G= , CM000679.1:g.74463766G= GRCh37
NC_000017.9:g.71975361G= NCBI36
NG_015976.1:g.19334G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000392492.8:c.-119G= MANE Select ENSP00000376282.2:n.-119G=
ENST00000250615.7:c.61-988G= ENSP00000250615.2:n.61-988G=
ENST00000392492.7:c.-119G= ENSP00000376282.2:n.-119G=
NM_001088.2:c.-119G= NP_001079.1:n.-119G=
NM_001166579.1:c.61-988G= NP_001160051.1:n.61-988G=
NR_110548.1:n.137G=
XM_011524415.1:c.-75-988G= XP_011522717.1:n.-75-988G=
XM_011524416.1:c.133-988G= XP_011522718.1:n.133-988G=
XM_011524417.1:c.133-988G= XP_011522719.1:n.133-988G=
XM_011524418.1:c.133-988G= XP_011522720.1:n.133-988G=
XM_011524419.1:c.133-988G= XP_011522721.1:n.133-988G=
XM_011524420.1:c.133-988G= XP_011522722.1:n.133-988G=
XM_011524421.1:c.133-988G= XP_011522723.1:n.133-988G=
XM_011524422.1:c.16-988G= XP_011522724.1:n.16-988G=
XM_011524423.1:c.-75-988G= XP_011522725.1:n.-75-988G=
XM_017024259.1:c.-949G= XP_016879748.1:n.-949G=
NM_001088.3:c.-119G= MANE Select NP_001079.1:n.-119G=
NR_110548.2:n.82G=
NM_001166579.2:c.61-988G= NP_001160051.1:n.61-988G=