Canonical Allele Identifier: CA627599487

Gene: AANAT

Linked Data

• dbSNP Id: rs1454628134
• gnomAD v2: 17-74465456-C-CA
• gnomAD v4: 17-76469374-C-CA
• MyVariant Identifiers: chr17:g.74465456_74465457insA (hg19) ; chr17:g.76469374_76469375insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76469375dup , CM000679.2:g.76469375dup	GRCh38
NC_000017.10:g.74465457dup , CM000679.1:g.74465457dup	GRCh37
NC_000017.9:g.71977052dup	NCBI36
NG_015976.1:g.21025dup
NG_032852.1:g.37053dup , LRG_532:g.37053dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392492.8:c.318+48dup MANE Select	ENSP00000376282.2:n.318+48dup
ENST00000250615.7:c.453+48dup	ENSP00000250615.2:n.453+48dup
ENST00000392492.7:c.318+48dup	ENSP00000376282.2:n.318+48dup
ENST00000585649.1:c.432+48dup	ENSP00000468717.1:n.432+48dup
ENST00000587798.1:c.*95+48dup	ENSP00000468239.1:n.*95+48dup
NM_001088.2:c.318+48dup	NP_001079.1:n.318+48dup
NM_001166579.1:c.453+48dup	NP_001160051.1:n.453+48dup
NR_110548.1:n.629+48dup
XM_011524415.1:c.318+48dup	XP_011522717.1:n.318+48dup
XM_011524416.1:c.525+48dup	XP_011522718.1:n.525+48dup
XM_011524417.1:c.525+48dup	XP_011522719.1:n.525+48dup
XM_011524418.1:c.525+48dup	XP_011522720.1:n.525+48dup
XM_011524419.1:c.525+48dup	XP_011522721.1:n.525+48dup
XM_011524420.1:c.525+48dup	XP_011522722.1:n.525+48dup
XM_011524421.1:c.525+48dup	XP_011522723.1:n.525+48dup
XM_011524422.1:c.408+48dup	XP_011522724.1:n.408+48dup
XM_011524423.1:c.318+48dup	XP_011522725.1:n.318+48dup
XM_017024259.1:c.432+48dup	XP_016879748.1:n.432+48dup
NM_001088.3:c.318+48dup MANE Select	NP_001079.1:n.318+48dup
NR_110548.2:n.574+48dup
NM_001166579.2:c.453+48dup	NP_001160051.1:n.453+48dup