Canonical Allele Identifier: CA401161005

Gene: AANAT

Linked Data

• MyVariant Identifiers: chr17:g.74465390A>T (hg19) ; chr17:g.76469308A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76469308A>T , CM000679.2:g.76469308A>T	GRCh38
NC_000017.10:g.74465390A>T , CM000679.1:g.74465390A>T	GRCh37
NC_000017.9:g.71976985A>T	NCBI36
NG_015976.1:g.20958A>T
NG_032852.1:g.37120T>A , LRG_532:g.37120T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392492.8:c.299A>T MANE Select	ENSP00000376282.2:p.Asp100Val
ENST00000250615.7:c.434A>T	ENSP00000250615.2:p.Asp145Val
ENST00000392492.7:c.299A>T	ENSP00000376282.2:p.Asp100Val
ENST00000585649.1:c.413A>T	ENSP00000468717.1:p.Asp138Val
ENST00000587798.1:c.*76A>T	ENSP00000468239.1:n.*76A>T
NM_001088.2:c.299A>T	NP_001079.1:p.Asp100Val
NM_001166579.1:c.434A>T	NP_001160051.1:p.Asp145Val
NR_110548.1:n.610A>T
XM_011524415.1:c.299A>T	XP_011522717.1:p.Asp100Val
XM_011524416.1:c.506A>T	XP_011522718.1:p.Asp169Val
XM_011524417.1:c.506A>T	XP_011522719.1:p.Asp169Val
XM_011524418.1:c.506A>T	XP_011522720.1:p.Asp169Val
XM_011524419.1:c.506A>T	XP_011522721.1:p.Asp169Val
XM_011524420.1:c.506A>T	XP_011522722.1:p.Asp169Val
XM_011524421.1:c.506A>T	XP_011522723.1:p.Asp169Val
XM_011524422.1:c.389A>T	XP_011522724.1:p.Asp130Val
XM_011524423.1:c.299A>T	XP_011522725.1:p.Asp100Val
XM_017024259.1:c.413A>T	XP_016879748.1:p.Asp138Val
NM_001088.3:c.299A>T MANE Select	NP_001079.1:p.Asp100Val
NR_110548.2:n.555A>T
NM_001166579.2:c.434A>T	NP_001160051.1:p.Asp145Val