Canonical Allele Identifier: CA369850570

Gene: AOC1

Linked Data

• MyVariant Identifiers: chr7:g.150558208C>T (hg19) ; chr7:g.150861120C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150861120C>T , CM000669.2:g.150861120C>T	GRCh38
NC_000007.13:g.150558208C>T , CM000669.1:g.150558208C>T	GRCh37
NC_000007.12:g.150189141C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000360937.9:c.2167C>T MANE Select	ENSP00000354193.4:p.Pro723Ser
ENST00000360937.8:c.2167C>T	ENSP00000354193.4:p.Pro723Ser
ENST00000416793.6:c.2224C>T	ENSP00000411613.2:p.Pro742Ser
ENST00000467291.5:c.2167C>T	ENSP00000418328.1:p.Pro723Ser
ENST00000480582.1:n.844C>T
ENST00000493429.5:c.2167C>T	ENSP00000418614.1:p.Pro723Ser
ENST00000619575.1:c.*24C>T	ENSP00000481717.1:n.*24C>T
ENST00000622116.4:c.*159C>T	ENSP00000481520.1:n.*159C>T
NM_001091.3:c.2167C>T	NP_001082.2:p.Pro723Ser
NM_001272072.1:c.2224C>T	NP_001259001.1:p.Pro742Ser
XM_011516008.1:c.2224C>T	XP_011514310.1:p.Pro742Ser
XM_011516009.1:c.2167C>T	XP_011514311.1:p.Pro723Ser
XR_928169.1:n.295+15889G>A
XR_928170.1:n.425+7496G>A
XR_928171.1:n.297+15889G>A
XM_017011944.1:c.2224C>T	XP_016867433.1:p.Pro742Ser
XM_017011945.1:c.2224C>T	XP_016867434.1:p.Pro742Ser
XM_017011946.2:c.2224C>T	XP_016867435.1:p.Pro742Ser
XM_017011947.1:c.2167C>T	XP_016867436.1:p.Pro723Ser
XR_928169.2:n.301+15889G>A
XR_928171.2:n.301+15889G>A
NM_001091.4:c.2167C>T MANE Select	NP_001082.2:p.Pro723Ser
NM_001272072.2:c.2224C>T	NP_001259001.1:p.Pro742Ser