Canonical Allele Identifier: CA1752388351

Gene: AOC1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150861170_150861171delinsTC , CM000669.2:g.150861170_150861171delinsTC	GRCh38
NC_000007.13:g.150558258_150558259delinsTC , CM000669.1:g.150558258_150558259delinsTC	GRCh37
NC_000007.12:g.150189191_150189192delinsTC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360937.9:c.2217_2218delinsTC MANE Select	ENSP00000354193.4:p.Pro739=
ENST00000360937.8:c.2217_2218delinsTC	ENSP00000354193.4:p.Pro739=
ENST00000416793.6:c.2274_2275delinsTC	ENSP00000411613.2:p.Pro758=
ENST00000467291.5:c.2217_2218delinsTC	ENSP00000418328.1:p.Pro739=
ENST00000480582.1:n.894_895delinsTC
ENST00000493429.5:c.2217_2218delinsTC	ENSP00000418614.1:p.Pro739=
ENST00000619575.1:c.*74_*75delinsTC	ENSP00000481717.1:n.*74_*75delinsTC
ENST00000622116.4:c.*209_*210delinsTC	ENSP00000481520.1:n.*209_*210delinsTC
NM_001091.3:c.2217_2218delinsTC	NP_001082.2:p.Pro739=
NM_001272072.1:c.2274_2275delinsTC	NP_001259001.1:p.Pro758=
XM_011516008.1:c.2274_2275delinsTC	XP_011514310.1:p.Pro758=
XM_011516009.1:c.2217_2218delinsTC	XP_011514311.1:p.Pro739=
XR_928169.1:n.295+15838_295+15839delinsGA
XR_928170.1:n.425+7445_425+7446delinsGA
XR_928171.1:n.297+15838_297+15839delinsGA
XM_017011944.1:c.2274_2275delinsTC	XP_016867433.1:p.Pro758=
XM_017011945.1:c.2274_2275delinsTC	XP_016867434.1:p.Pro758=
XM_017011946.2:c.2274_2275delinsTC	XP_016867435.1:p.Pro758=
XM_017011947.1:c.2217_2218delinsTC	XP_016867436.1:p.Pro739=
XR_928169.2:n.301+15838_301+15839delinsGA
XR_928171.2:n.301+15838_301+15839delinsGA
NM_001091.4:c.2217_2218delinsTC MANE Select	NP_001082.2:p.Pro739=
NM_001272072.2:c.2274_2275delinsTC	NP_001259001.1:p.Pro758=