Canonical Allele Identifier: CA1752396452

Gene: AOC1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150857509_150857510delinsGC , CM000669.2:g.150857509_150857510delinsGC	GRCh38
NC_000007.13:g.150554597_150554598delinsGC , CM000669.1:g.150554597_150554598delinsGC	GRCh37
NC_000007.12:g.150185530_150185531delinsGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360937.9:c.1039_1040delinsGC MANE Select	ENSP00000354193.4:p.Ala347=
ENST00000360937.8:c.1039_1040delinsGC	ENSP00000354193.4:p.Ala347=
ENST00000416793.6:c.1039_1040delinsGC	ENSP00000411613.2:p.Ala347=
ENST00000467291.5:c.1039_1040delinsGC	ENSP00000418328.1:p.Ala347=
ENST00000493429.5:c.1039_1040delinsGC	ENSP00000418614.1:p.Ala347=
ENST00000619575.1:c.1036_1037delinsGC	ENSP00000481717.1:p.Ala346=
ENST00000622116.4:c.-384_-383delinsGC	ENSP00000481520.1:n.-384_-383delinsGC
NM_001091.3:c.1039_1040delinsGC	NP_001082.2:p.Ala347=
NM_001272072.1:c.1039_1040delinsGC	NP_001259001.1:p.Ala347=
XM_011516008.1:c.1039_1040delinsGC	XP_011514310.1:p.Ala347=
XM_011516009.1:c.1039_1040delinsGC	XP_011514311.1:p.Ala347=
XR_928169.1:n.296-16065_296-16064delinsGC
XR_928170.1:n.425+11106_425+11107delinsGC
XR_928171.1:n.298-16065_298-16064delinsGC
XM_017011944.1:c.1039_1040delinsGC	XP_016867433.1:p.Ala347=
XM_017011945.1:c.1039_1040delinsGC	XP_016867434.1:p.Ala347=
XM_017011946.2:c.1039_1040delinsGC	XP_016867435.1:p.Ala347=
XM_017011947.1:c.1039_1040delinsGC	XP_016867436.1:p.Ala347=
XR_928169.2:n.302-16065_302-16064delinsGC
XR_928171.2:n.302-16065_302-16064delinsGC
NM_001091.4:c.1039_1040delinsGC MANE Select	NP_001082.2:p.Ala347=
NM_001272072.2:c.1039_1040delinsGC	NP_001259001.1:p.Ala347=