Canonical Allele Identifier: CA1752395630

Gene: AOC1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150857223_150857224delinsGA , CM000669.2:g.150857223_150857224delinsGA	GRCh38
NC_000007.13:g.150554311_150554312delinsGA , CM000669.1:g.150554311_150554312delinsGA	GRCh37
NC_000007.12:g.150185244_150185245delinsGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360937.9:c.753_754delinsGA MANE Select	ENSP00000354193.4:p.Arg251=
ENST00000360937.8:c.753_754delinsGA	ENSP00000354193.4:p.Arg251=
ENST00000416793.6:c.753_754delinsGA	ENSP00000411613.2:p.Arg251=
ENST00000467291.5:c.753_754delinsGA	ENSP00000418328.1:p.Arg251=
ENST00000483043.1:c.753_754delinsGA	ENSP00000417392.1:p.Arg251=
ENST00000493429.5:c.753_754delinsGA	ENSP00000418614.1:p.Arg251=
ENST00000619575.1:c.753_754delinsGA	ENSP00000481717.1:p.Arg251=
ENST00000622116.4:c.-670_-669delinsGA	ENSP00000481520.1:n.-670_-669delinsGA
NM_001091.3:c.753_754delinsGA	NP_001082.2:p.Arg251=
NM_001272072.1:c.753_754delinsGA	NP_001259001.1:p.Arg251=
XM_011516008.1:c.753_754delinsGA	XP_011514310.1:p.Arg251=
XM_011516009.1:c.753_754delinsGA	XP_011514311.1:p.Arg251=
XR_928169.1:n.296-15779_296-15778delinsTC
XR_928170.1:n.425+11392_425+11393delinsTC
XR_928171.1:n.298-15779_298-15778delinsTC
XM_017011944.1:c.753_754delinsGA	XP_016867433.1:p.Arg251=
XM_017011945.1:c.753_754delinsGA	XP_016867434.1:p.Arg251=
XM_017011946.2:c.753_754delinsGA	XP_016867435.1:p.Arg251=
XM_017011947.1:c.753_754delinsGA	XP_016867436.1:p.Arg251=
XR_928169.2:n.302-15779_302-15778delinsTC
XR_928171.2:n.302-15779_302-15778delinsTC
NM_001091.4:c.753_754delinsGA MANE Select	NP_001082.2:p.Arg251=
NM_001272072.2:c.753_754delinsGA	NP_001259001.1:p.Arg251=