Canonical Allele Identifier: CA2639995843

Gene: AANAT

Linked Data

• gnomAD v4: 17-76469425-C-CAGG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76469425_76469426insAGG , CM000679.2:g.76469425_76469426insAGG	GRCh38
NC_000017.10:g.74465507_74465508insAGG , CM000679.1:g.74465507_74465508insAGG	GRCh37
NC_000017.9:g.71977102_71977103insAGG	NCBI36
NG_015976.1:g.21075_21076insAGG
NG_032852.1:g.37002_37003insCCT , LRG_532:g.37002_37003insCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392492.8:c.318+98_318+99insAGG MANE Select	ENSP00000376282.2:n.318+98_318+99insAGG
ENST00000250615.7:c.453+98_453+99insAGG	ENSP00000250615.2:n.453+98_453+99insAGG
ENST00000392492.7:c.318+98_318+99insAGG	ENSP00000376282.2:n.318+98_318+99insAGG
ENST00000585649.1:c.432+98_432+99insAGG	ENSP00000468717.1:n.432+98_432+99insAGG
ENST00000587798.1:c.*95+98_*95+99insAGG	ENSP00000468239.1:n.*95+98_*95+99insAGG
NM_001088.2:c.318+98_318+99insAGG	NP_001079.1:n.318+98_318+99insAGG
NM_001166579.1:c.453+98_453+99insAGG	NP_001160051.1:n.453+98_453+99insAGG
NR_110548.1:n.629+98_629+99insAGG
XM_011524415.1:c.318+98_318+99insAGG	XP_011522717.1:n.318+98_318+99insAGG
XM_011524416.1:c.525+98_525+99insAGG	XP_011522718.1:n.525+98_525+99insAGG
XM_011524417.1:c.525+98_525+99insAGG	XP_011522719.1:n.525+98_525+99insAGG
XM_011524418.1:c.525+98_525+99insAGG	XP_011522720.1:n.525+98_525+99insAGG
XM_011524419.1:c.525+98_525+99insAGG	XP_011522721.1:n.525+98_525+99insAGG
XM_011524420.1:c.525+98_525+99insAGG	XP_011522722.1:n.525+98_525+99insAGG
XM_011524421.1:c.525+98_525+99insAGG	XP_011522723.1:n.525+98_525+99insAGG
XM_011524422.1:c.408+98_408+99insAGG	XP_011522724.1:n.408+98_408+99insAGG
XM_011524423.1:c.318+98_318+99insAGG	XP_011522725.1:n.318+98_318+99insAGG
XM_017024259.1:c.432+98_432+99insAGG	XP_016879748.1:n.432+98_432+99insAGG
NM_001088.3:c.318+98_318+99insAGG MANE Select	NP_001079.1:n.318+98_318+99insAGG
NR_110548.2:n.574+98_574+99insAGG
NM_001166579.2:c.453+98_453+99insAGG	NP_001160051.1:n.453+98_453+99insAGG