Canonical Allele Identifier: CA401161197

Gene: AANAT

Linked Data

• MyVariant Identifiers: chr17:g.74465814C>T (hg19) ; chr17:g.76469732C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76469732C>T , CM000679.2:g.76469732C>T	GRCh38
NC_000017.10:g.74465814C>T , CM000679.1:g.74465814C>T	GRCh37
NC_000017.9:g.71977409C>T	NCBI36
NG_015976.1:g.21382C>T
NG_032852.1:g.36696G>A , LRG_532:g.36696G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000392492.8:c.386C>T MANE Select	ENSP00000376282.2:p.Ala129Val
ENST00000250615.7:c.521C>T	ENSP00000250615.2:p.Ala174Val
ENST00000392492.7:c.386C>T	ENSP00000376282.2:p.Ala129Val
ENST00000587798.1:c.*163C>T	ENSP00000468239.1:n.*163C>T
NM_001088.2:c.386C>T	NP_001079.1:p.Ala129Val
NM_001166579.1:c.521C>T	NP_001160051.1:p.Ala174Val
NR_110548.1:n.697C>T
XM_011524415.1:c.386C>T	XP_011522717.1:p.Ala129Val
XM_011524416.1:c.593C>T	XP_011522718.1:p.Ala198Val
XM_011524417.1:c.593C>T	XP_011522719.1:p.Ala198Val
XM_011524418.1:c.593C>T	XP_011522720.1:p.Ala198Val
XM_011524419.1:c.593C>T	XP_011522721.1:p.Ala198Val
XM_011524420.1:c.593C>T	XP_011522722.1:p.Ala198Val
XM_011524421.1:c.593C>T	XP_011522723.1:p.Ala198Val
XM_011524422.1:c.476C>T	XP_011522724.1:p.Ala159Val
XM_011524423.1:c.386C>T	XP_011522725.1:p.Ala129Val
XM_017024259.1:c.500C>T	XP_016879748.1:p.Ala167Val
NM_001088.3:c.386C>T MANE Select	NP_001079.1:p.Ala129Val
NR_110548.2:n.642C>T
NM_001166579.2:c.521C>T	NP_001160051.1:p.Ala174Val