Canonical Allele Identifier: CA369845840

Gene: AOC1

Linked Data

• MyVariant Identifiers: chr7:g.150553655T>G (hg19) ; chr7:g.150856567T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150856567T>G , CM000669.2:g.150856567T>G	GRCh38
NC_000007.13:g.150553655T>G , CM000669.1:g.150553655T>G	GRCh37
NC_000007.12:g.150184588T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360937.9:c.97T>G MANE Select	ENSP00000354193.4:p.Phe33Val
ENST00000360937.8:c.97T>G	ENSP00000354193.4:p.Phe33Val
ENST00000416793.6:c.97T>G	ENSP00000411613.2:p.Phe33Val
ENST00000460213.1:c.97T>G	ENSP00000418557.1:p.Phe33Val
ENST00000467291.5:c.97T>G	ENSP00000418328.1:p.Phe33Val
ENST00000483043.1:c.97T>G	ENSP00000417392.1:p.Phe33Val
ENST00000493429.5:c.97T>G	ENSP00000418614.1:p.Phe33Val
ENST00000619575.1:c.97T>G	ENSP00000481717.1:p.Phe33Val
ENST00000622116.4:c.-1326T>G	ENSP00000481520.1:n.-1326T>G
NM_001091.3:c.97T>G	NP_001082.2:p.Phe33Val
NM_001272072.1:c.97T>G	NP_001259001.1:p.Phe33Val
XM_011516008.1:c.97T>G	XP_011514310.1:p.Phe33Val
XM_011516009.1:c.97T>G	XP_011514311.1:p.Phe33Val
XR_928169.1:n.296-15122A>C
XR_928170.1:n.425+12049A>C
XR_928171.1:n.298-15122A>C
XM_017011944.1:c.97T>G	XP_016867433.1:p.Phe33Val
XM_017011945.1:c.97T>G	XP_016867434.1:p.Phe33Val
XM_017011946.2:c.97T>G	XP_016867435.1:p.Phe33Val
XM_017011947.1:c.97T>G	XP_016867436.1:p.Phe33Val
XR_928169.2:n.302-15122A>C
XR_928171.2:n.302-15122A>C
NM_001091.4:c.97T>G MANE Select	NP_001082.2:p.Phe33Val
NM_001272072.2:c.97T>G	NP_001259001.1:p.Phe33Val