Canonical Allele Identifier: CA835208065

Gene: AOC1

Linked Data

• dbSNP Id: rs1403665771
• MyVariant Identifiers: chr7:g.150558359_150558361del (hg19) ; chr7:g.150861271_150861273del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150861273_150861275del , CM000669.2:g.150861273_150861275del	GRCh38
NC_000007.13:g.150558361_150558363del , CM000669.1:g.150558361_150558363del	GRCh37
NC_000007.12:g.150189294_150189296del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360937.9:c.*64_*66del MANE Select	ENSP00000354193.4:n.*64_*66del
ENST00000360937.8:c.*64_*66del	ENSP00000354193.4:n.*64_*66del
ENST00000416793.6:c.*64_*66del	ENSP00000411613.2:n.*64_*66del
ENST00000467291.5:c.*64_*66del	ENSP00000418328.1:n.*64_*66del
ENST00000493429.5:c.*64_*66del	ENSP00000418614.1:n.*64_*66del
ENST00000619575.1:c.*177_*179del	ENSP00000481717.1:n.*177_*179del
ENST00000622116.4:c.*312_*314del	ENSP00000481520.1:n.*312_*314del
NM_001091.3:c.*64_*66del	NP_001082.2:n.*64_*66del
NM_001272072.1:c.*64_*66del	NP_001259001.1:n.*64_*66del
XM_011516008.1:c.*64_*66del	XP_011514310.1:n.*64_*66del
XM_011516009.1:c.*64_*66del	XP_011514311.1:n.*64_*66del
XR_928169.1:n.295+15736_295+15738del
XR_928170.1:n.425+7343_425+7345del
XR_928171.1:n.297+15736_297+15738del
XM_017011944.1:c.*64_*66del	XP_016867433.1:n.*64_*66del
XM_017011945.1:c.*64_*66del	XP_016867434.1:n.*64_*66del
XM_017011946.2:c.*64_*66del	XP_016867435.1:n.*64_*66del
XM_017011947.1:c.*64_*66del	XP_016867436.1:n.*64_*66del
XR_928169.2:n.301+15736_301+15738del
XR_928171.2:n.301+15736_301+15738del
NM_001091.4:c.*64_*66del MANE Select	NP_001082.2:n.*64_*66del
NM_001272072.2:c.*64_*66del	NP_001259001.1:n.*64_*66del