Canonical Allele Identifier: CA502066636

Gene: AANAT

Linked Data

• MyVariant Identifiers: chr17:g.74465815C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76469733C>G , CM000679.2:g.76469733C>G	GRCh38
NC_000017.10:g.74465815C>G , CM000679.1:g.74465815C>G	GRCh37
NC_000017.9:g.71977410C>G	NCBI36
NG_015976.1:g.21383C>G
NG_032852.1:g.36695G>C , LRG_532:g.36695G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000392492.8:c.387C>G MANE Select	ENSP00000376282.2:p.Ala129=
ENST00000250615.7:c.522C>G	ENSP00000250615.2:p.Ala174=
ENST00000392492.7:c.387C>G	ENSP00000376282.2:p.Ala129=
ENST00000587798.1:c.*164C>G	ENSP00000468239.1:n.*164C>G
NM_001088.2:c.387C>G	NP_001079.1:p.Ala129=
NM_001166579.1:c.522C>G	NP_001160051.1:p.Ala174=
NR_110548.1:n.698C>G
XM_011524415.1:c.387C>G	XP_011522717.1:p.Ala129=
XM_011524416.1:c.594C>G	XP_011522718.1:p.Ala198=
XM_011524417.1:c.594C>G	XP_011522719.1:p.Ala198=
XM_011524418.1:c.594C>G	XP_011522720.1:p.Ala198=
XM_011524419.1:c.594C>G	XP_011522721.1:p.Ala198=
XM_011524420.1:c.594C>G	XP_011522722.1:p.Ala198=
XM_011524421.1:c.594C>G	XP_011522723.1:p.Ala198=
XM_011524422.1:c.477C>G	XP_011522724.1:p.Ala159=
XM_011524423.1:c.387C>G	XP_011522725.1:p.Ala129=
XM_017024259.1:c.501C>G	XP_016879748.1:p.Ala167=
NM_001088.3:c.387C>G MANE Select	NP_001079.1:p.Ala129=
NR_110548.2:n.643C>G
NM_001166579.2:c.522C>G	NP_001160051.1:p.Ala174=