Canonical Allele Identifier: CA340911045
Community Standard Title: NM_000959.4(PTGFR):c.449A>T (p.Lys150Ile)
Gene: PTGFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.78493192A>T , CM000663.2:g.78493192A>T GRCh38
NC_000001.10:g.78958877A>T , CM000663.1:g.78958877A>T GRCh37
NC_000001.9:g.78731465A>T NCBI36
NG_052997.1:g.7219A>T

Transcript Alleles

HGVS Amino-acid Change
NM_000959.4:c.449A>T MANE Select NP_000950.1:p.Lys150Ile
ENST00000370757.8:c.449A>T MANE Select ENSP00000359793.3:p.Lys150Ile
NM_000959.3:c.449A>T NP_000950.1:p.Lys150Ile
NM_001039585.1:c.449A>T NP_001034674.1:p.Lys150Ile
NM_001039585.2:c.449A>T NP_001034674.1:p.Lys150Ile
ENST00000370756.3:c.449A>T ENSP00000359792.3:p.Lys150Ile
ENST00000370757.7:c.449A>T ENSP00000359793.3:p.Lys150Ile
ENST00000370758.5:c.449A>T ENSP00000359794.1:p.Lys150Ile
ENST00000497923.5:c.449A>T ENSP00000432599.1:p.Lys150Ile
XM_006710781.2:c.449A>T XP_006710844.1:p.Lys150Ile
XM_017001873.1:c.449A>T XP_016857362.1:p.Lys150Ile
XR_001737338.1:n.784A>T
XR_426624.2:n.784A>T
XR_946715.1:n.784A>T
XR_946715.2:n.784A>T