Canonical Allele Identifier: CA1192431747
Gene: PHGDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119726904A= , CM000663.2:g.119726904A= GRCh38
NC_000001.10:g.120269527A= , CM000663.1:g.120269527A= GRCh37
NC_000001.9:g.120071050A= NCBI36
NG_009188.1:g.20109A=

Transcript Alleles

HGVS Amino-acid change
ENST00000369409.9:c.410A= ENSP00000358417.5:p.Lys137=
ENST00000462324.2:n.493A=
ENST00000641023.2:c.410A= MANE Select ENSP00000493175.1:p.Lys137=
ENST00000641074.1:c.410A= ENSP00000493446.1:p.Lys137=
ENST00000641115.1:c.410A= ENSP00000493264.1:p.Lys137=
ENST00000641213.1:c.*63A= ENSP00000493079.1:n.*63A=
ENST00000641247.1:c.*129A= ENSP00000492955.1:n.*129A=
ENST00000641272.1:c.344A= ENSP00000493432.1:p.Lys115=
ENST00000641314.1:n.395A=
ENST00000641371.1:c.324A= ENSP00000493305.1:p.Glu108=
ENST00000641375.1:c.*246A= ENSP00000493089.1:n.*246A=
ENST00000641491.1:c.*63A= ENSP00000493187.1:n.*63A=
ENST00000641570.1:c.*129A= ENSP00000493213.1:n.*129A=
ENST00000641573.1:n.498A=
ENST00000641587.1:c.*121A= ENSP00000493453.1:n.*121A=
ENST00000641597.1:c.410A= ENSP00000493382.1:p.Lys137=
ENST00000641711.1:n.634A=
ENST00000641756.1:c.*154A= ENSP00000493147.1:n.*154A=
ENST00000641811.1:c.166A=
ENST00000641847.1:n.269A=
ENST00000641891.1:c.*236A= ENSP00000493288.1:n.*236A=
ENST00000641927.1:n.350A=
ENST00000641947.1:c.410A= ENSP00000492994.1:p.Lys137=
ENST00000642021.1:n.532A=
ENST00000642041.1:c.*449A= ENSP00000493415.1:n.*449A=
ENST00000369407.3:c.308A= ENSP00000358415.3:p.Lys103=
ENST00000369409.8:c.410A= ENSP00000358417.4:p.Lys137=
ENST00000462324.1:n.678A=
ENST00000493622.5:n.599A=
NM_006623.3:c.410A= NP_006614.2:p.Lys137=
XM_011541226.1:c.632A= XP_011539528.1:p.Lys211=
XM_011541227.1:c.554A= XP_011539529.1:p.Lys185=
XM_011541228.1:c.521A= XP_011539530.1:p.Lys174=
XM_011541229.1:c.347A= XP_011539531.1:p.Lys116=
XM_011541230.1:c.125A= XP_011539532.1:p.Lys42=
XM_011541231.1:c.116A= XP_011539533.1:p.Lys39=
XM_011541226.2:c.632A= XP_011539528.1:p.Lys211=
XM_011541227.2:c.554A= XP_011539529.1:p.Lys185=
XM_011541228.2:c.521A= XP_011539530.1:p.Lys174=
XM_011541231.2:c.116A= XP_011539533.1:p.Lys39=
XM_024446338.1:c.521A= XP_024302106.1:p.Lys174=
NM_006623.4:c.410A= MANE Select NP_006614.2:p.Lys137=