Canonical Allele Identifier: CA294177739

Gene: AANAT

Linked Data

• dbSNP Id: rs868453416
• MyVariant Identifiers: chr17:g.74465351A>T (hg19) ; chr17:g.76469269A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76469269A>T , CM000679.2:g.76469269A>T	GRCh38
NC_000017.10:g.74465351A>T , CM000679.1:g.74465351A>T	GRCh37
NC_000017.9:g.71976946A>T	NCBI36
NG_015976.1:g.20919A>T
NG_032852.1:g.37159T>A , LRG_532:g.37159T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392492.8:c.260A>T MANE Select	ENSP00000376282.2:p.Glu87Val
ENST00000250615.7:c.395A>T	ENSP00000250615.2:p.Glu132Val
ENST00000392492.7:c.260A>T	ENSP00000376282.2:p.Glu87Val
ENST00000585649.1:c.374A>T	ENSP00000468717.1:p.Glu125Val
ENST00000587798.1:c.*37A>T	ENSP00000468239.1:n.*37A>T
NM_001088.2:c.260A>T	NP_001079.1:p.Glu87Val
NM_001166579.1:c.395A>T	NP_001160051.1:p.Glu132Val
NR_110548.1:n.571A>T
XM_011524415.1:c.260A>T	XP_011522717.1:p.Glu87Val
XM_011524416.1:c.467A>T	XP_011522718.1:p.Glu156Val
XM_011524417.1:c.467A>T	XP_011522719.1:p.Glu156Val
XM_011524418.1:c.467A>T	XP_011522720.1:p.Glu156Val
XM_011524419.1:c.467A>T	XP_011522721.1:p.Glu156Val
XM_011524420.1:c.467A>T	XP_011522722.1:p.Glu156Val
XM_011524421.1:c.467A>T	XP_011522723.1:p.Glu156Val
XM_011524422.1:c.350A>T	XP_011522724.1:p.Glu117Val
XM_011524423.1:c.260A>T	XP_011522725.1:p.Glu87Val
XM_017024259.1:c.374A>T	XP_016879748.1:p.Glu125Val
NM_001088.3:c.260A>T MANE Select	NP_001079.1:p.Glu87Val
NR_110548.2:n.516A>T
NM_001166579.2:c.395A>T	NP_001160051.1:p.Glu132Val