Canonical Allele Identifier: CA2685597564

Gene: AOC1

Linked Data

• gnomAD v4: 7-150861213-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150861213G>T , CM000669.2:g.150861213G>T	GRCh38
NC_000007.13:g.150558301G>T , CM000669.1:g.150558301G>T	GRCh37
NC_000007.12:g.150189234G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000360937.9:c.*4G>T MANE Select	ENSP00000354193.4:n.*4G>T
ENST00000360937.8:c.*4G>T	ENSP00000354193.4:n.*4G>T
ENST00000416793.6:c.*4G>T	ENSP00000411613.2:n.*4G>T
ENST00000467291.5:c.*4G>T	ENSP00000418328.1:n.*4G>T
ENST00000480582.1:n.937G>T
ENST00000493429.5:c.*4G>T	ENSP00000418614.1:n.*4G>T
ENST00000619575.1:c.*117G>T	ENSP00000481717.1:n.*117G>T
ENST00000622116.4:c.*252G>T	ENSP00000481520.1:n.*252G>T
NM_001091.3:c.*4G>T	NP_001082.2:n.*4G>T
NM_001272072.1:c.*4G>T	NP_001259001.1:n.*4G>T
XM_011516008.1:c.*4G>T	XP_011514310.1:n.*4G>T
XM_011516009.1:c.*4G>T	XP_011514311.1:n.*4G>T
XR_928169.1:n.295+15796C>A
XR_928170.1:n.425+7403C>A
XR_928171.1:n.297+15796C>A
XM_017011944.1:c.*4G>T	XP_016867433.1:n.*4G>T
XM_017011945.1:c.*4G>T	XP_016867434.1:n.*4G>T
XM_017011946.2:c.*4G>T	XP_016867435.1:n.*4G>T
XM_017011947.1:c.*4G>T	XP_016867436.1:n.*4G>T
XR_928169.2:n.301+15796C>A
XR_928171.2:n.301+15796C>A
NM_001091.4:c.*4G>T MANE Select	NP_001082.2:n.*4G>T
NM_001272072.2:c.*4G>T	NP_001259001.1:n.*4G>T