Canonical Allele Identifier: CA8786536
Gene: AANAT HGNC NCBI

Linked Data

dbSNP Id: rs577400794

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.76469299C>T , CM000679.2:g.76469299C>T GRCh38
NC_000017.10:g.74465381C>T , CM000679.1:g.74465381C>T GRCh37
NC_000017.9:g.71976976C>T NCBI36
NG_015976.1:g.20949C>T
NG_032852.1:g.37129G>A , LRG_532:g.37129G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000392492.8:c.290C>T MANE Select ENSP00000376282.2:p.Ser97Leu
ENST00000250615.7:c.425C>T ENSP00000250615.2:p.Ser142Leu
ENST00000392492.7:c.290C>T ENSP00000376282.2:p.Ser97Leu
ENST00000585649.1:c.404C>T ENSP00000468717.1:p.Ser135Leu
ENST00000587798.1:c.*67C>T ENSP00000468239.1:n.*67C>T
NM_001088.2:c.290C>T NP_001079.1:p.Ser97Leu
NM_001166579.1:c.425C>T NP_001160051.1:p.Ser142Leu
NR_110548.1:n.601C>T
XM_011524415.1:c.290C>T XP_011522717.1:p.Ser97Leu
XM_011524416.1:c.497C>T XP_011522718.1:p.Ser166Leu
XM_011524417.1:c.497C>T XP_011522719.1:p.Ser166Leu
XM_011524418.1:c.497C>T XP_011522720.1:p.Ser166Leu
XM_011524419.1:c.497C>T XP_011522721.1:p.Ser166Leu
XM_011524420.1:c.497C>T XP_011522722.1:p.Ser166Leu
XM_011524421.1:c.497C>T XP_011522723.1:p.Ser166Leu
XM_011524422.1:c.380C>T XP_011522724.1:p.Ser127Leu
XM_011524423.1:c.290C>T XP_011522725.1:p.Ser97Leu
XM_017024259.1:c.404C>T XP_016879748.1:p.Ser135Leu
NM_001088.3:c.290C>T MANE Select NP_001079.1:p.Ser97Leu
NR_110548.2:n.546C>T
NM_001166579.2:c.425C>T NP_001160051.1:p.Ser142Leu