Canonical Allele Identifier: CA369850731

Gene: AOC1

Linked Data

• MyVariant Identifiers: chr7:g.150558280A>G (hg19) ; chr7:g.150861192A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150861192A>G , CM000669.2:g.150861192A>G	GRCh38
NC_000007.13:g.150558280A>G , CM000669.1:g.150558280A>G	GRCh37
NC_000007.12:g.150189213A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360937.9:c.2239A>G MANE Select	ENSP00000354193.4:p.Thr747Ala
ENST00000360937.8:c.2239A>G	ENSP00000354193.4:p.Thr747Ala
ENST00000416793.6:c.2296A>G	ENSP00000411613.2:p.Thr766Ala
ENST00000467291.5:c.2239A>G	ENSP00000418328.1:p.Thr747Ala
ENST00000480582.1:n.916A>G
ENST00000493429.5:c.2239A>G	ENSP00000418614.1:p.Thr747Ala
ENST00000619575.1:c.*96A>G	ENSP00000481717.1:n.*96A>G
ENST00000622116.4:c.*231A>G	ENSP00000481520.1:n.*231A>G
NM_001091.3:c.2239A>G	NP_001082.2:p.Thr747Ala
NM_001272072.1:c.2296A>G	NP_001259001.1:p.Thr766Ala
XM_011516008.1:c.2296A>G	XP_011514310.1:p.Thr766Ala
XM_011516009.1:c.2239A>G	XP_011514311.1:p.Thr747Ala
XR_928169.1:n.295+15817T>C
XR_928170.1:n.425+7424T>C
XR_928171.1:n.297+15817T>C
XM_017011944.1:c.2296A>G	XP_016867433.1:p.Thr766Ala
XM_017011945.1:c.2296A>G	XP_016867434.1:p.Thr766Ala
XM_017011946.2:c.2296A>G	XP_016867435.1:p.Thr766Ala
XM_017011947.1:c.2239A>G	XP_016867436.1:p.Thr747Ala
XR_928169.2:n.301+15817T>C
XR_928171.2:n.301+15817T>C
NM_001091.4:c.2239A>G MANE Select	NP_001082.2:p.Thr747Ala
NM_001272072.2:c.2296A>G	NP_001259001.1:p.Thr766Ala