Canonical Allele Identifier: CA401161046

Gene: AANAT

Linked Data

• MyVariant Identifiers: chr17:g.74465408A>C (hg19) ; chr17:g.76469326A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76469326A>C , CM000679.2:g.76469326A>C	GRCh38
NC_000017.10:g.74465408A>C , CM000679.1:g.74465408A>C	GRCh37
NC_000017.9:g.71977003A>C	NCBI36
NG_015976.1:g.20976A>C
NG_032852.1:g.37102T>G , LRG_532:g.37102T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392492.8:c.317A>C MANE Select	ENSP00000376282.2:p.Gln106Pro
ENST00000250615.7:c.452A>C	ENSP00000250615.2:p.Gln151Pro
ENST00000392492.7:c.317A>C	ENSP00000376282.2:p.Gln106Pro
ENST00000585649.1:c.431A>C	ENSP00000468717.1:p.Gln144Pro
ENST00000587798.1:c.*94A>C	ENSP00000468239.1:n.*94A>C
NM_001088.2:c.317A>C	NP_001079.1:p.Gln106Pro
NM_001166579.1:c.452A>C	NP_001160051.1:p.Gln151Pro
NR_110548.1:n.628A>C
XM_011524415.1:c.317A>C	XP_011522717.1:p.Gln106Pro
XM_011524416.1:c.524A>C	XP_011522718.1:p.Gln175Pro
XM_011524417.1:c.524A>C	XP_011522719.1:p.Gln175Pro
XM_011524418.1:c.524A>C	XP_011522720.1:p.Gln175Pro
XM_011524419.1:c.524A>C	XP_011522721.1:p.Gln175Pro
XM_011524420.1:c.524A>C	XP_011522722.1:p.Gln175Pro
XM_011524421.1:c.524A>C	XP_011522723.1:p.Gln175Pro
XM_011524422.1:c.407A>C	XP_011522724.1:p.Gln136Pro
XM_011524423.1:c.317A>C	XP_011522725.1:p.Gln106Pro
XM_017024259.1:c.431A>C	XP_016879748.1:p.Gln144Pro
NM_001088.3:c.317A>C MANE Select	NP_001079.1:p.Gln106Pro
NR_110548.2:n.573A>C
NM_001166579.2:c.452A>C	NP_001160051.1:p.Gln151Pro