Canonical Allele Identifier: CA2276011955
Gene: AANAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.76469736C= , CM000679.2:g.76469736C= GRCh38
NC_000017.10:g.74465818C= , CM000679.1:g.74465818C= GRCh37
NC_000017.9:g.71977413C= NCBI36
NG_015976.1:g.21386C=
NG_032852.1:g.36692G= , LRG_532:g.36692G=

Transcript Alleles

HGVS Amino-acid change
ENST00000392492.8:c.390C= MANE Select ENSP00000376282.2:p.Phe130=
ENST00000250615.7:c.525C= ENSP00000250615.2:p.Phe175=
ENST00000392492.7:c.390C= ENSP00000376282.2:p.Phe130=
ENST00000587798.1:c.*167C= ENSP00000468239.1:n.*167C=
NM_001088.2:c.390C= NP_001079.1:p.Phe130=
NM_001166579.1:c.525C= NP_001160051.1:p.Phe175=
NR_110548.1:n.701C=
XM_011524415.1:c.390C= XP_011522717.1:p.Phe130=
XM_011524416.1:c.597C= XP_011522718.1:p.Phe199=
XM_011524417.1:c.597C= XP_011522719.1:p.Phe199=
XM_011524418.1:c.597C= XP_011522720.1:p.Phe199=
XM_011524419.1:c.597C= XP_011522721.1:p.Phe199=
XM_011524420.1:c.597C= XP_011522722.1:p.Phe199=
XM_011524421.1:c.597C= XP_011522723.1:p.Phe199=
XM_011524422.1:c.480C= XP_011522724.1:p.Phe160=
XM_011524423.1:c.390C= XP_011522725.1:p.Phe130=
XM_017024259.1:c.504C= XP_016879748.1:p.Phe168=
NM_001088.3:c.390C= MANE Select NP_001079.1:p.Phe130=
NR_110548.2:n.646C=
NM_001166579.2:c.525C= NP_001160051.1:p.Phe175=