Canonical Allele Identifier: CA458871122

Gene: AOC1

Linked Data

• dbSNP Id: rs1331583587
• gnomAD v2: 7-150555019-C-T
• gnomAD v3: 7-150857931-C-T
• gnomAD v4: 7-150857931-C-T
• MyVariant Identifiers: chr7:g.150555019C>T (hg19) ; chr7:g.150857931C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150857931C>T , CM000669.2:g.150857931C>T	GRCh38
NC_000007.13:g.150555019C>T , CM000669.1:g.150555019C>T	GRCh37
NC_000007.12:g.150185952C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360937.9:c.1461C>T MANE Select	ENSP00000354193.4:p.Ala487=
ENST00000360937.8:c.1461C>T	ENSP00000354193.4:p.Ala487=
ENST00000416793.6:c.1461C>T	ENSP00000411613.2:p.Ala487=
ENST00000467291.5:c.1461C>T	ENSP00000418328.1:p.Ala487=
ENST00000493429.5:c.1461C>T	ENSP00000418614.1:p.Ala487=
ENST00000619575.1:c.1458C>T	ENSP00000481717.1:p.Ala486=
ENST00000622116.4:c.39C>T	ENSP00000481520.1:p.Ala13=
NM_001091.3:c.1461C>T	NP_001082.2:p.Ala487=
NM_001272072.1:c.1461C>T	NP_001259001.1:p.Ala487=
XM_011516008.1:c.1461C>T	XP_011514310.1:p.Ala487=
XM_011516009.1:c.1461C>T	XP_011514311.1:p.Ala487=
XR_928169.1:n.296-16486G>A
XR_928170.1:n.425+10685G>A
XR_928171.1:n.298-16486G>A
XM_017011944.1:c.1461C>T	XP_016867433.1:p.Ala487=
XM_017011945.1:c.1461C>T	XP_016867434.1:p.Ala487=
XM_017011946.2:c.1461C>T	XP_016867435.1:p.Ala487=
XM_017011947.1:c.1461C>T	XP_016867436.1:p.Ala487=
XR_928169.2:n.302-16486G>A
XR_928171.2:n.302-16486G>A
NM_001091.4:c.1461C>T MANE Select	NP_001082.2:p.Ala487=
NM_001272072.2:c.1461C>T	NP_001259001.1:p.Ala487=