Canonical Allele Identifier: CA369850591

Gene: AOC1

Linked Data

• dbSNP Id: rs1005694705
• MyVariant Identifiers: chr7:g.150558218T>A (hg19) ; chr7:g.150861130T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150861130T>A , CM000669.2:g.150861130T>A	GRCh38
NC_000007.13:g.150558218T>A , CM000669.1:g.150558218T>A	GRCh37
NC_000007.12:g.150189151T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360937.9:c.2177T>A MANE Select	ENSP00000354193.4:p.Val726Asp
ENST00000360937.8:c.2177T>A	ENSP00000354193.4:p.Val726Asp
ENST00000416793.6:c.2234T>A	ENSP00000411613.2:p.Val745Asp
ENST00000467291.5:c.2177T>A	ENSP00000418328.1:p.Val726Asp
ENST00000480582.1:n.854T>A
ENST00000493429.5:c.2177T>A	ENSP00000418614.1:p.Val726Asp
ENST00000619575.1:c.*34T>A	ENSP00000481717.1:n.*34T>A
ENST00000622116.4:c.*169T>A	ENSP00000481520.1:n.*169T>A
NM_001091.3:c.2177T>A	NP_001082.2:p.Val726Asp
NM_001272072.1:c.2234T>A	NP_001259001.1:p.Val745Asp
XM_011516008.1:c.2234T>A	XP_011514310.1:p.Val745Asp
XM_011516009.1:c.2177T>A	XP_011514311.1:p.Val726Asp
XR_928169.1:n.295+15879A>T
XR_928170.1:n.425+7486A>T
XR_928171.1:n.297+15879A>T
XM_017011944.1:c.2234T>A	XP_016867433.1:p.Val745Asp
XM_017011945.1:c.2234T>A	XP_016867434.1:p.Val745Asp
XM_017011946.2:c.2234T>A	XP_016867435.1:p.Val745Asp
XM_017011947.1:c.2177T>A	XP_016867436.1:p.Val726Asp
XR_928169.2:n.301+15879A>T
XR_928171.2:n.301+15879A>T
NM_001091.4:c.2177T>A MANE Select	NP_001082.2:p.Val726Asp
NM_001272072.2:c.2234T>A	NP_001259001.1:p.Val745Asp