Canonical Allele Identifier: CA919897819

Gene: AANAT

Linked Data

• dbSNP Id: rs1567866224
• gnomAD v4: 17-76467548-C-CCCAGGTGGGGTGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76467548_76467549insCCAGGTGGGGTGGG , CM000679.2:g.76467548_76467549insCCAGGTGGGGTGGG	GRCh38
NC_000017.10:g.74463630_74463631insCCAGGTGGGGTGGG , CM000679.1:g.74463630_74463631insCCAGGTGGGGTGGG	GRCh37
NC_000017.9:g.71975225_71975226insCCAGGTGGGGTGGG	NCBI36
NG_015976.1:g.19198_19199insCCAGGTGGGGTGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000250615.7:c.61-1124_61-1123insCCAGGTGGGGTGGG	ENSP00000250615.2:n.61-1124_61-1123insCCAGGTGGGGTGGG
NM_001088.2:c.-255_-254insCCAGGTGGGGTGGG	NP_001079.1:n.-255_-254insCCAGGTGGGGTGGG
NM_001166579.1:c.61-1124_61-1123insCCAGGTGGGGTGGG	NP_001160051.1:n.61-1124_61-1123insCCAGGTGGGGTGGG
NR_110548.1:n.1_2insCCAGGTGGGGTGGG
XM_011524415.1:c.-75-1124_-75-1123insCCAGGTGGGGTGGG	XP_011522717.1:n.-75-1124_-75-1123insCCAGGTGGGGTGGG
XM_011524416.1:c.133-1124_133-1123insCCAGGTGGGGTGGG	XP_011522718.1:n.133-1124_133-1123insCCAGGTGGGGTGGG
XM_011524417.1:c.133-1124_133-1123insCCAGGTGGGGTGGG	XP_011522719.1:n.133-1124_133-1123insCCAGGTGGGGTGGG
XM_011524418.1:c.133-1124_133-1123insCCAGGTGGGGTGGG	XP_011522720.1:n.133-1124_133-1123insCCAGGTGGGGTGGG
XM_011524419.1:c.133-1124_133-1123insCCAGGTGGGGTGGG	XP_011522721.1:n.133-1124_133-1123insCCAGGTGGGGTGGG
XM_011524420.1:c.133-1124_133-1123insCCAGGTGGGGTGGG	XP_011522722.1:n.133-1124_133-1123insCCAGGTGGGGTGGG
XM_011524421.1:c.133-1124_133-1123insCCAGGTGGGGTGGG	XP_011522723.1:n.133-1124_133-1123insCCAGGTGGGGTGGG
XM_011524422.1:c.16-1124_16-1123insCCAGGTGGGGTGGG	XP_011522724.1:n.16-1124_16-1123insCCAGGTGGGGTGGG
XM_011524423.1:c.-75-1124_-75-1123insCCAGGTGGGGTGGG	XP_011522725.1:n.-75-1124_-75-1123insCCAGGTGGGGTGGG
XM_017024259.1:c.-1085_-1084insCCAGGTGGGGTGGG	XP_016879748.1:n.-1085_-1084insCCAGGTGGGGTGGG
NM_001166579.2:c.61-1124_61-1123insCCAGGTGGGGTGGG	NP_001160051.1:n.61-1124_61-1123insCCAGGTGGGGTGGG