Canonical Allele Identifier: CA2276011715

Gene: AANAT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76469282_76469294delinsGGCCTTCATCATC , CM000679.2:g.76469282_76469294delinsGGCCTTCATCATC	GRCh38
NC_000017.10:g.74465364_74465376delinsGGCCTTCATCATC , CM000679.1:g.74465364_74465376delinsGGCCTTCATCATC	GRCh37
NC_000017.9:g.71976959_71976971delinsGGCCTTCATCATC	NCBI36
NG_015976.1:g.20932_20944delinsGGCCTTCATCATC
NG_032852.1:g.37134_37146delinsGATGATGAAGGCC , LRG_532:g.37134_37146delinsGATGATGAAGGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392492.8:c.273_285delinsGGCCTTCATCATC MANE Select	ENSP00000376282.2:p.Val91=
ENST00000250615.7:c.408_420delinsGGCCTTCATCATC	ENSP00000250615.2:p.Val136=
ENST00000392492.7:c.273_285delinsGGCCTTCATCATC	ENSP00000376282.2:p.Val91=
ENST00000585649.1:c.387_399delinsGGCCTTCATCATC	ENSP00000468717.1:p.Val129=
ENST00000587798.1:c.*50_*62delinsGGCCTTCATCATC	ENSP00000468239.1:n.*50_*62delinsGGCCTTCATCATC
NM_001088.2:c.273_285delinsGGCCTTCATCATC	NP_001079.1:p.Val91=
NM_001166579.1:c.408_420delinsGGCCTTCATCATC	NP_001160051.1:p.Val136=
NR_110548.1:n.584_596delinsGGCCTTCATCATC
XM_011524415.1:c.273_285delinsGGCCTTCATCATC	XP_011522717.1:p.Val91=
XM_011524416.1:c.480_492delinsGGCCTTCATCATC	XP_011522718.1:p.Val160=
XM_011524417.1:c.480_492delinsGGCCTTCATCATC	XP_011522719.1:p.Val160=
XM_011524418.1:c.480_492delinsGGCCTTCATCATC	XP_011522720.1:p.Val160=
XM_011524419.1:c.480_492delinsGGCCTTCATCATC	XP_011522721.1:p.Val160=
XM_011524420.1:c.480_492delinsGGCCTTCATCATC	XP_011522722.1:p.Val160=
XM_011524421.1:c.480_492delinsGGCCTTCATCATC	XP_011522723.1:p.Val160=
XM_011524422.1:c.363_375delinsGGCCTTCATCATC	XP_011522724.1:p.Val121=
XM_011524423.1:c.273_285delinsGGCCTTCATCATC	XP_011522725.1:p.Val91=
XM_017024259.1:c.387_399delinsGGCCTTCATCATC	XP_016879748.1:p.Val129=
NM_001088.3:c.273_285delinsGGCCTTCATCATC MANE Select	NP_001079.1:p.Val91=
NR_110548.2:n.529_541delinsGGCCTTCATCATC
NM_001166579.2:c.408_420delinsGGCCTTCATCATC	NP_001160051.1:p.Val136=