Canonical Allele Identifier: CA1192431740
Gene: PHGDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119726876A= , CM000663.2:g.119726876A= GRCh38
NC_000001.10:g.120269499A= , CM000663.1:g.120269499A= GRCh37
NC_000001.9:g.120071022A= NCBI36
NG_009188.1:g.20081A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369409.9:c.382A= ENSP00000358417.5:p.Met128=
ENST00000462324.2:n.465A=
ENST00000641023.2:c.382A= MANE Select ENSP00000493175.1:p.Met128=
ENST00000641074.1:c.382A= ENSP00000493446.1:p.Met128=
ENST00000641115.1:c.382A= ENSP00000493264.1:p.Met128=
ENST00000641213.1:c.*35A= ENSP00000493079.1:n.*35A=
ENST00000641247.1:c.*101A= ENSP00000492955.1:n.*101A=
ENST00000641272.1:c.316A= ENSP00000493432.1:p.Met106=
ENST00000641314.1:n.367A=
ENST00000641371.1:c.296A= ENSP00000493305.1:p.Asp99=
ENST00000641375.1:c.*218A= ENSP00000493089.1:n.*218A=
ENST00000641491.1:c.*35A= ENSP00000493187.1:n.*35A=
ENST00000641513.1:c.*126A= ENSP00000493398.1:n.*126A=
ENST00000641570.1:c.*101A= ENSP00000493213.1:n.*101A=
ENST00000641573.1:n.470A=
ENST00000641587.1:c.*93A= ENSP00000493453.1:n.*93A=
ENST00000641597.1:c.382A= ENSP00000493382.1:p.Met128=
ENST00000641711.1:n.606A=
ENST00000641756.1:c.*126A= ENSP00000493147.1:n.*126A=
ENST00000641811.1:c.138A=
ENST00000641847.1:n.241A=
ENST00000641891.1:c.*208A= ENSP00000493288.1:n.*208A=
ENST00000641927.1:n.322A=
ENST00000641947.1:c.382A= ENSP00000492994.1:p.Met128=
ENST00000642021.1:n.504A=
ENST00000642041.1:c.*421A= ENSP00000493415.1:n.*421A=
ENST00000369407.3:c.280A= ENSP00000358415.3:p.Met94=
ENST00000369409.8:c.382A= ENSP00000358417.4:p.Met128=
ENST00000462324.1:n.650A=
ENST00000493622.5:n.571A=
NM_006623.3:c.382A= NP_006614.2:p.Met128=
XM_011541226.1:c.604A= XP_011539528.1:p.Met202=
XM_011541227.1:c.526A= XP_011539529.1:p.Met176=
XM_011541228.1:c.493A= XP_011539530.1:p.Met165=
XM_011541229.1:c.319A= XP_011539531.1:p.Met107=
XM_011541230.1:c.97A= XP_011539532.1:p.Met33=
XM_011541231.1:c.88A= XP_011539533.1:p.Met30=
XM_011541226.2:c.604A= XP_011539528.1:p.Met202=
XM_011541227.2:c.526A= XP_011539529.1:p.Met176=
XM_011541228.2:c.493A= XP_011539530.1:p.Met165=
XM_011541231.2:c.88A= XP_011539533.1:p.Met30=
XM_024446338.1:c.493A= XP_024302106.1:p.Met165=
NM_006623.4:c.382A= MANE Select NP_006614.2:p.Met128=