Canonical Allele Identifier: CA2038523137

Gene: PTGES3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56671929C>G , CM000674.2:g.56671929C>G	GRCh38
NC_000012.11:g.57065713C>G , CM000674.1:g.57065713C>G	GRCh37
NC_000012.10:g.55351980C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262033.11:c.187-82G>C MANE Select	ENSP00000262033.6:n.187-82G>C
ENST00000262033.10:c.187-82G>C	ENSP00000262033.6:n.187-82G>C
ENST00000414274.7:c.187-82G>C	ENSP00000405299.3:n.187-82G>C
ENST00000436399.6:c.186+811G>C	ENSP00000402385.2:n.186+811G>C
ENST00000448157.6:c.187-82G>C	ENSP00000414892.2:n.187-82G>C
ENST00000456859.2:c.117-120G>C	ENSP00000389090.2:n.117-120G>C
ENST00000537473.2:n.933-82G>C
ENST00000614328.4:c.199-82G>C	ENSP00000482075.1:n.199-82G>C
NM_001282601.1:c.187-82G>C	NP_001269530.1:n.187-82G>C
NM_001282602.1:c.187-82G>C	NP_001269531.1:n.187-82G>C
NM_001282603.1:c.186+811G>C	NP_001269532.1:n.186+811G>C
NM_001282604.1:c.199-82G>C	NP_001269533.1:n.199-82G>C
NM_001282605.1:c.187-82G>C	NP_001269534.1:n.187-82G>C
NM_006601.6:c.187-82G>C	NP_006592.3:n.187-82G>C
NR_104219.1:n.933-82G>C
XM_005268576.3:c.199-82G>C	XP_005268633.1:n.199-82G>C
XM_006719199.1:c.199-82G>C	XP_006719262.1:n.199-82G>C
XM_011537773.1:c.187-82G>C	XP_011536075.1:n.187-82G>C
XM_011537774.1:c.199-82G>C	XP_011536076.1:n.199-82G>C
XM_005268576.5:c.199-82G>C	XP_005268633.1:n.199-82G>C
XM_006719199.2:c.199-82G>C	XP_006719262.1:n.199-82G>C
XM_011537773.2:c.187-82G>C	XP_011536075.1:n.187-82G>C
XM_011537774.2:c.199-82G>C	XP_011536076.1:n.199-82G>C
XM_017018716.1:c.199-82G>C	XP_016874205.1:n.199-82G>C
NM_006601.7:c.187-82G>C MANE Select	NP_006592.3:n.187-82G>C
NM_001282601.2:c.187-82G>C	NP_001269530.1:n.187-82G>C
NM_001282602.2:c.187-82G>C	NP_001269531.1:n.187-82G>C
NM_001282603.2:c.186+811G>C	NP_001269532.1:n.186+811G>C
NM_001282605.2:c.187-82G>C	NP_001269534.1:n.187-82G>C
NR_104219.2:n.1220-82G>C
NM_001282604.2:c.199-82G>C	NP_001269533.1:n.199-82G>C