Canonical Allele Identifier: CA369847328

Gene: AOC1

Linked Data

• dbSNP Id: rs370158924
• gnomAD v3: 7-150857268-G-C
• gnomAD v4: 7-150857268-G-C
• MyVariant Identifiers: chr7:g.150554356G>C (hg19) ; chr7:g.150857268G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150857268G>C , CM000669.2:g.150857268G>C	GRCh38
NC_000007.13:g.150554356G>C , CM000669.1:g.150554356G>C	GRCh37
NC_000007.12:g.150185289G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360937.9:c.798G>C MANE Select	ENSP00000354193.4:p.Pro266=
ENST00000360937.8:c.798G>C	ENSP00000354193.4:p.Pro266=
ENST00000416793.6:c.798G>C	ENSP00000411613.2:p.Pro266=
ENST00000467291.5:c.798G>C	ENSP00000418328.1:p.Pro266=
ENST00000483043.1:c.798G>C	ENSP00000417392.1:p.Pro266=
ENST00000493429.5:c.798G>C	ENSP00000418614.1:p.Pro266=
ENST00000619575.1:c.797G>C	ENSP00000481717.1:p.Arg266Pro
ENST00000622116.4:c.-625G>C	ENSP00000481520.1:n.-625G>C
NM_001091.3:c.798G>C	NP_001082.2:p.Pro266=
NM_001272072.1:c.798G>C	NP_001259001.1:p.Pro266=
XM_011516008.1:c.798G>C	XP_011514310.1:p.Pro266=
XM_011516009.1:c.798G>C	XP_011514311.1:p.Pro266=
XR_928169.1:n.296-15823C>G
XR_928170.1:n.425+11348C>G
XR_928171.1:n.298-15823C>G
XM_017011944.1:c.798G>C	XP_016867433.1:p.Pro266=
XM_017011945.1:c.798G>C	XP_016867434.1:p.Pro266=
XM_017011946.2:c.798G>C	XP_016867435.1:p.Pro266=
XM_017011947.1:c.798G>C	XP_016867436.1:p.Pro266=
XR_928169.2:n.302-15823C>G
XR_928171.2:n.302-15823C>G
NM_001091.4:c.798G>C MANE Select	NP_001082.2:p.Pro266=
NM_001272072.2:c.798G>C	NP_001259001.1:p.Pro266=