Canonical Allele Identifier: CA502066638

Gene: AANAT

Linked Data

• dbSNP Id: rs1418766096
• gnomAD v2: 17-74465818-C-T
• gnomAD v4: 17-76469736-C-T
• MyVariant Identifiers: chr17:g.74465818C>T (hg19) ; chr17:g.76469736C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76469736C>T , CM000679.2:g.76469736C>T	GRCh38
NC_000017.10:g.74465818C>T , CM000679.1:g.74465818C>T	GRCh37
NC_000017.9:g.71977413C>T	NCBI36
NG_015976.1:g.21386C>T
NG_032852.1:g.36692G>A , LRG_532:g.36692G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000392492.8:c.390C>T MANE Select	ENSP00000376282.2:p.Phe130=
ENST00000250615.7:c.525C>T	ENSP00000250615.2:p.Phe175=
ENST00000392492.7:c.390C>T	ENSP00000376282.2:p.Phe130=
ENST00000587798.1:c.*167C>T	ENSP00000468239.1:n.*167C>T
NM_001088.2:c.390C>T	NP_001079.1:p.Phe130=
NM_001166579.1:c.525C>T	NP_001160051.1:p.Phe175=
NR_110548.1:n.701C>T
XM_011524415.1:c.390C>T	XP_011522717.1:p.Phe130=
XM_011524416.1:c.597C>T	XP_011522718.1:p.Phe199=
XM_011524417.1:c.597C>T	XP_011522719.1:p.Phe199=
XM_011524418.1:c.597C>T	XP_011522720.1:p.Phe199=
XM_011524419.1:c.597C>T	XP_011522721.1:p.Phe199=
XM_011524420.1:c.597C>T	XP_011522722.1:p.Phe199=
XM_011524421.1:c.597C>T	XP_011522723.1:p.Phe199=
XM_011524422.1:c.480C>T	XP_011522724.1:p.Phe160=
XM_011524423.1:c.390C>T	XP_011522725.1:p.Phe130=
XM_017024259.1:c.504C>T	XP_016879748.1:p.Phe168=
NM_001088.3:c.390C>T MANE Select	NP_001079.1:p.Phe130=
NR_110548.2:n.646C>T
NM_001166579.2:c.525C>T	NP_001160051.1:p.Phe175=