Canonical Allele Identifier: CA8786527
Gene: AANAT HGNC NCBI

Linked Data

dbSNP Id: rs371535966

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.76469265G>A , CM000679.2:g.76469265G>A GRCh38
NC_000017.10:g.74465347G>A , CM000679.1:g.74465347G>A GRCh37
NC_000017.9:g.71976942G>A NCBI36
NG_015976.1:g.20915G>A
NG_032852.1:g.37163C>T , LRG_532:g.37163C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000392492.8:c.256G>A MANE Select ENSP00000376282.2:p.Glu86Lys
ENST00000250615.7:c.391G>A ENSP00000250615.2:p.Glu131Lys
ENST00000392492.7:c.256G>A ENSP00000376282.2:p.Glu86Lys
ENST00000585649.1:c.370G>A ENSP00000468717.1:p.Glu124Lys
ENST00000587798.1:c.*33G>A ENSP00000468239.1:n.*33G>A
NM_001088.2:c.256G>A NP_001079.1:p.Glu86Lys
NM_001166579.1:c.391G>A NP_001160051.1:p.Glu131Lys
NR_110548.1:n.567G>A
XM_011524415.1:c.256G>A XP_011522717.1:p.Glu86Lys
XM_011524416.1:c.463G>A XP_011522718.1:p.Glu155Lys
XM_011524417.1:c.463G>A XP_011522719.1:p.Glu155Lys
XM_011524418.1:c.463G>A XP_011522720.1:p.Glu155Lys
XM_011524419.1:c.463G>A XP_011522721.1:p.Glu155Lys
XM_011524420.1:c.463G>A XP_011522722.1:p.Glu155Lys
XM_011524421.1:c.463G>A XP_011522723.1:p.Glu155Lys
XM_011524422.1:c.346G>A XP_011522724.1:p.Glu116Lys
XM_011524423.1:c.256G>A XP_011522725.1:p.Glu86Lys
XM_017024259.1:c.370G>A XP_016879748.1:p.Glu124Lys
NM_001088.3:c.256G>A MANE Select NP_001079.1:p.Glu86Lys
NR_110548.2:n.512G>A
NM_001166579.2:c.391G>A NP_001160051.1:p.Glu131Lys