Canonical Allele Identifier: CA501886089

Gene: AANAT

Linked Data

• MyVariant Identifiers: chr17:g.74465364G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76469282G>T , CM000679.2:g.76469282G>T	GRCh38
NC_000017.10:g.74465364G>T , CM000679.1:g.74465364G>T	GRCh37
NC_000017.9:g.71976959G>T	NCBI36
NG_015976.1:g.20932G>T
NG_032852.1:g.37146C>A , LRG_532:g.37146C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392492.8:c.273G>T MANE Select	ENSP00000376282.2:p.Val91=
ENST00000250615.7:c.408G>T	ENSP00000250615.2:p.Val136=
ENST00000392492.7:c.273G>T	ENSP00000376282.2:p.Val91=
ENST00000585649.1:c.387G>T	ENSP00000468717.1:p.Val129=
ENST00000587798.1:c.*50G>T	ENSP00000468239.1:n.*50G>T
NM_001088.2:c.273G>T	NP_001079.1:p.Val91=
NM_001166579.1:c.408G>T	NP_001160051.1:p.Val136=
NR_110548.1:n.584G>T
XM_011524415.1:c.273G>T	XP_011522717.1:p.Val91=
XM_011524416.1:c.480G>T	XP_011522718.1:p.Val160=
XM_011524417.1:c.480G>T	XP_011522719.1:p.Val160=
XM_011524418.1:c.480G>T	XP_011522720.1:p.Val160=
XM_011524419.1:c.480G>T	XP_011522721.1:p.Val160=
XM_011524420.1:c.480G>T	XP_011522722.1:p.Val160=
XM_011524421.1:c.480G>T	XP_011522723.1:p.Val160=
XM_011524422.1:c.363G>T	XP_011522724.1:p.Val121=
XM_011524423.1:c.273G>T	XP_011522725.1:p.Val91=
XM_017024259.1:c.387G>T	XP_016879748.1:p.Val129=
NM_001088.3:c.273G>T MANE Select	NP_001079.1:p.Val91=
NR_110548.2:n.529G>T
NM_001166579.2:c.408G>T	NP_001160051.1:p.Val136=