Canonical Allele Identifier: CA401160957

Gene: AANAT

Linked Data

• dbSNP Id: rs2073483694
• MyVariant Identifiers: chr17:g.74465365G>A (hg19) ; chr17:g.76469283G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76469283G>A , CM000679.2:g.76469283G>A	GRCh38
NC_000017.10:g.74465365G>A , CM000679.1:g.74465365G>A	GRCh37
NC_000017.9:g.71976960G>A	NCBI36
NG_015976.1:g.20933G>A
NG_032852.1:g.37145C>T , LRG_532:g.37145C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392492.8:c.274G>A MANE Select	ENSP00000376282.2:p.Ala92Thr
ENST00000250615.7:c.409G>A	ENSP00000250615.2:p.Ala137Thr
ENST00000392492.7:c.274G>A	ENSP00000376282.2:p.Ala92Thr
ENST00000585649.1:c.388G>A	ENSP00000468717.1:p.Ala130Thr
ENST00000587798.1:c.*51G>A	ENSP00000468239.1:n.*51G>A
NM_001088.2:c.274G>A	NP_001079.1:p.Ala92Thr
NM_001166579.1:c.409G>A	NP_001160051.1:p.Ala137Thr
NR_110548.1:n.585G>A
XM_011524415.1:c.274G>A	XP_011522717.1:p.Ala92Thr
XM_011524416.1:c.481G>A	XP_011522718.1:p.Ala161Thr
XM_011524417.1:c.481G>A	XP_011522719.1:p.Ala161Thr
XM_011524418.1:c.481G>A	XP_011522720.1:p.Ala161Thr
XM_011524419.1:c.481G>A	XP_011522721.1:p.Ala161Thr
XM_011524420.1:c.481G>A	XP_011522722.1:p.Ala161Thr
XM_011524421.1:c.481G>A	XP_011522723.1:p.Ala161Thr
XM_011524422.1:c.364G>A	XP_011522724.1:p.Ala122Thr
XM_011524423.1:c.274G>A	XP_011522725.1:p.Ala92Thr
XM_017024259.1:c.388G>A	XP_016879748.1:p.Ala130Thr
NM_001088.3:c.274G>A MANE Select	NP_001079.1:p.Ala92Thr
NR_110548.2:n.530G>A
NM_001166579.2:c.409G>A	NP_001160051.1:p.Ala137Thr