Canonical Allele Identifier: CA2639993353

Gene: AANAT

Linked Data

• gnomAD v4: 17-76467570-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76467570A>G , CM000679.2:g.76467570A>G	GRCh38
NC_000017.10:g.74463652A>G , CM000679.1:g.74463652A>G	GRCh37
NC_000017.9:g.71975247A>G	NCBI36
NG_015976.1:g.19220A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000250615.7:c.61-1102A>G	ENSP00000250615.2:n.61-1102A>G
ENST00000392492.7:c.-233A>G	ENSP00000376282.2:n.-233A>G
NM_001088.2:c.-233A>G	NP_001079.1:n.-233A>G
NM_001166579.1:c.61-1102A>G	NP_001160051.1:n.61-1102A>G
NR_110548.1:n.23A>G
XM_011524415.1:c.-75-1102A>G	XP_011522717.1:n.-75-1102A>G
XM_011524416.1:c.133-1102A>G	XP_011522718.1:n.133-1102A>G
XM_011524417.1:c.133-1102A>G	XP_011522719.1:n.133-1102A>G
XM_011524418.1:c.133-1102A>G	XP_011522720.1:n.133-1102A>G
XM_011524419.1:c.133-1102A>G	XP_011522721.1:n.133-1102A>G
XM_011524420.1:c.133-1102A>G	XP_011522722.1:n.133-1102A>G
XM_011524421.1:c.133-1102A>G	XP_011522723.1:n.133-1102A>G
XM_011524422.1:c.16-1102A>G	XP_011522724.1:n.16-1102A>G
XM_011524423.1:c.-75-1102A>G	XP_011522725.1:n.-75-1102A>G
XM_017024259.1:c.-1063A>G	XP_016879748.1:n.-1063A>G
NM_001166579.2:c.61-1102A>G	NP_001160051.1:n.61-1102A>G