Canonical Allele Identifier: CA2639993523

Gene: AANAT

Linked Data

• gnomAD v4: 17-76467670-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76467670G>A , CM000679.2:g.76467670G>A	GRCh38
NC_000017.10:g.74463752G>A , CM000679.1:g.74463752G>A	GRCh37
NC_000017.9:g.71975347G>A	NCBI36
NG_015976.1:g.19320G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392492.8:c.-133G>A MANE Select	ENSP00000376282.2:n.-133G>A
ENST00000250615.7:c.61-1002G>A	ENSP00000250615.2:n.61-1002G>A
ENST00000392492.7:c.-133G>A	ENSP00000376282.2:n.-133G>A
NM_001088.2:c.-133G>A	NP_001079.1:n.-133G>A
NM_001166579.1:c.61-1002G>A	NP_001160051.1:n.61-1002G>A
NR_110548.1:n.123G>A
XM_011524415.1:c.-75-1002G>A	XP_011522717.1:n.-75-1002G>A
XM_011524416.1:c.133-1002G>A	XP_011522718.1:n.133-1002G>A
XM_011524417.1:c.133-1002G>A	XP_011522719.1:n.133-1002G>A
XM_011524418.1:c.133-1002G>A	XP_011522720.1:n.133-1002G>A
XM_011524419.1:c.133-1002G>A	XP_011522721.1:n.133-1002G>A
XM_011524420.1:c.133-1002G>A	XP_011522722.1:n.133-1002G>A
XM_011524421.1:c.133-1002G>A	XP_011522723.1:n.133-1002G>A
XM_011524422.1:c.16-1002G>A	XP_011522724.1:n.16-1002G>A
XM_011524423.1:c.-75-1002G>A	XP_011522725.1:n.-75-1002G>A
XM_017024259.1:c.-963G>A	XP_016879748.1:n.-963G>A
NM_001088.3:c.-133G>A MANE Select	NP_001079.1:n.-133G>A
NR_110548.2:n.68G>A
NM_001166579.2:c.61-1002G>A	NP_001160051.1:n.61-1002G>A