Canonical Allele Identifier: CA2639996182

Gene: AANAT

Linked Data

• gnomAD v4: 17-76469564-C-CCG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76469564_76469565insCG , CM000679.2:g.76469564_76469565insCG	GRCh38
NC_000017.10:g.74465646_74465647insCG , CM000679.1:g.74465646_74465647insCG	GRCh37
NC_000017.9:g.71977241_71977242insCG	NCBI36
NG_015976.1:g.21214_21215insCG
NG_032852.1:g.36863_36864insCG , LRG_532:g.36863_36864insCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392492.8:c.319-101_319-100insCG MANE Select	ENSP00000376282.2:n.319-101_319-100insCG
ENST00000250615.7:c.454-101_454-100insCG	ENSP00000250615.2:n.454-101_454-100insCG
ENST00000392492.7:c.319-101_319-100insCG	ENSP00000376282.2:n.319-101_319-100insCG
ENST00000585649.1:c.433-101_433-100insCG	ENSP00000468717.1:n.433-101_433-100insCG
ENST00000587798.1:c.*96-101_*96-100insCG	ENSP00000468239.1:n.*96-101_*96-100insCG
NM_001088.2:c.319-101_319-100insCG	NP_001079.1:n.319-101_319-100insCG
NM_001166579.1:c.454-101_454-100insCG	NP_001160051.1:n.454-101_454-100insCG
NR_110548.1:n.630-101_630-100insCG
XM_011524415.1:c.319-101_319-100insCG	XP_011522717.1:n.319-101_319-100insCG
XM_011524416.1:c.526-101_526-100insCG	XP_011522718.1:n.526-101_526-100insCG
XM_011524417.1:c.526-101_526-100insCG	XP_011522719.1:n.526-101_526-100insCG
XM_011524418.1:c.526-101_526-100insCG	XP_011522720.1:n.526-101_526-100insCG
XM_011524419.1:c.526-101_526-100insCG	XP_011522721.1:n.526-101_526-100insCG
XM_011524420.1:c.526-101_526-100insCG	XP_011522722.1:n.526-101_526-100insCG
XM_011524421.1:c.526-101_526-100insCG	XP_011522723.1:n.526-101_526-100insCG
XM_011524422.1:c.409-101_409-100insCG	XP_011522724.1:n.409-101_409-100insCG
XM_011524423.1:c.319-101_319-100insCG	XP_011522725.1:n.319-101_319-100insCG
XM_017024259.1:c.433-101_433-100insCG	XP_016879748.1:n.433-101_433-100insCG
NM_001088.3:c.319-101_319-100insCG MANE Select	NP_001079.1:n.319-101_319-100insCG
NR_110548.2:n.575-101_575-100insCG
NM_001166579.2:c.454-101_454-100insCG	NP_001160051.1:n.454-101_454-100insCG