Canonical Allele Identifier: CA1177870570

Gene: PTGFR

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.78521617T>A , CM000663.2:g.78521617T>A	GRCh38
NC_000001.10:g.78987302T>A , CM000663.1:g.78987302T>A	GRCh37
NC_000001.9:g.78759890T>A	NCBI36
NG_052997.1:g.35644T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370757.8:c.799-14789T>A MANE Select	ENSP00000359793.3:n.799-14789T>A
ENST00000370756.3:c.870-14789T>A	ENSP00000359792.3:n.870-14789T>A
ENST00000370757.7:c.799-14789T>A	ENSP00000359793.3:n.799-14789T>A
ENST00000370758.5:c.799-14789T>A	ENSP00000359794.1:n.799-14789T>A
ENST00000497923.5:c.870-10596T>A	ENSP00000432599.1:n.870-10596T>A
NM_000959.3:c.799-14789T>A	NP_000950.1:n.799-14789T>A
NM_001039585.1:c.870-14789T>A	NP_001034674.1:n.870-14789T>A
XM_006710781.2:c.799-14789T>A	XP_006710844.1:n.799-14789T>A
XR_426624.2:n.1347-14789T>A
XR_001737338.1:n.1134-10596T>A
NM_000959.4:c.799-14789T>A MANE Select	NP_000950.1:n.799-14789T>A
NM_001039585.2:c.870-14789T>A	NP_001034674.1:n.870-14789T>A