Canonical Allele Identifier: CA1192431464
Gene: PHGDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119726390_119726391delinsAT , CM000663.2:g.119726390_119726391delinsAT GRCh38
NC_000001.10:g.120269013_120269014delinsAT , CM000663.1:g.120269013_120269014delinsAT GRCh37
NC_000001.9:g.120070536_120070537delinsAT NCBI36
NG_009188.1:g.19595_19596delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000369409.9:c.357-461_357-460delinsAT ENSP00000358417.5:n.357-461_357-460delinsAT
ENST00000462324.2:n.440-461_440-460delinsAT
ENST00000641023.2:c.357-461_357-460delinsAT MANE Select ENSP00000493175.1:n.357-461_357-460delinsAT
ENST00000641074.1:c.357-461_357-460delinsAT ENSP00000493446.1:n.357-461_357-460delinsAT
ENST00000641115.1:c.357-461_357-460delinsAT ENSP00000493264.1:n.357-461_357-460delinsAT
ENST00000641213.1:c.*10-461_*10-460delinsAT ENSP00000493079.1:n.*10-461_*10-460delinsAT
ENST00000641247.1:c.*76-461_*76-460delinsAT ENSP00000492955.1:n.*76-461_*76-460delinsAT
ENST00000641272.1:c.291-461_291-460delinsAT ENSP00000493432.1:n.291-461_291-460delinsAT
ENST00000641314.1:n.342-461_342-460delinsAT
ENST00000641371.1:c.271-461_271-460delinsAT ENSP00000493305.1:n.271-461_271-460delinsAT
ENST00000641375.1:c.*193-461_*193-460delinsAT ENSP00000493089.1:n.*193-461_*193-460delinsAT
ENST00000641491.1:c.*10-461_*10-460delinsAT ENSP00000493187.1:n.*10-461_*10-460delinsAT
ENST00000641513.1:c.*101-461_*101-460delinsAT ENSP00000493398.1:n.*101-461_*101-460delinsAT
ENST00000641570.1:c.*76-461_*76-460delinsAT ENSP00000493213.1:n.*76-461_*76-460delinsAT
ENST00000641573.1:n.445-461_445-460delinsAT
ENST00000641587.1:c.*68-461_*68-460delinsAT ENSP00000493453.1:n.*68-461_*68-460delinsAT
ENST00000641597.1:c.357-461_357-460delinsAT ENSP00000493382.1:n.357-461_357-460delinsAT
ENST00000641711.1:n.581-461_581-460delinsAT
ENST00000641756.1:c.*101-461_*101-460delinsAT ENSP00000493147.1:n.*101-461_*101-460delinsAT
ENST00000641811.1:c.113-461_113-460delinsAT
ENST00000641891.1:c.*183-461_*183-460delinsAT ENSP00000493288.1:n.*183-461_*183-460delinsAT
ENST00000641927.1:n.297-461_297-460delinsAT
ENST00000641947.1:c.357-461_357-460delinsAT ENSP00000492994.1:n.357-461_357-460delinsAT
ENST00000642021.1:n.479-461_479-460delinsAT
ENST00000642041.1:c.*396-461_*396-460delinsAT ENSP00000493415.1:n.*396-461_*396-460delinsAT
ENST00000369407.3:c.255-461_255-460delinsAT ENSP00000358415.3:n.255-461_255-460delinsAT
ENST00000369409.8:c.357-461_357-460delinsAT ENSP00000358417.4:n.357-461_357-460delinsAT
ENST00000462324.1:n.625-461_625-460delinsAT
ENST00000493622.5:n.546-461_546-460delinsAT
NM_006623.3:c.357-461_357-460delinsAT NP_006614.2:n.357-461_357-460delinsAT
XM_011541226.1:c.579-461_579-460delinsAT XP_011539528.1:n.579-461_579-460delinsAT
XM_011541227.1:c.501-461_501-460delinsAT XP_011539529.1:n.501-461_501-460delinsAT
XM_011541228.1:c.468-461_468-460delinsAT XP_011539530.1:n.468-461_468-460delinsAT
XM_011541229.1:c.294-461_294-460delinsAT XP_011539531.1:n.294-461_294-460delinsAT
XM_011541230.1:c.72-461_72-460delinsAT XP_011539532.1:n.72-461_72-460delinsAT
XM_011541231.1:c.63-461_63-460delinsAT XP_011539533.1:n.63-461_63-460delinsAT
XM_011541226.2:c.579-461_579-460delinsAT XP_011539528.1:n.579-461_579-460delinsAT
XM_011541227.2:c.501-461_501-460delinsAT XP_011539529.1:n.501-461_501-460delinsAT
XM_011541228.2:c.468-461_468-460delinsAT XP_011539530.1:n.468-461_468-460delinsAT
XM_011541231.2:c.63-461_63-460delinsAT XP_011539533.1:n.63-461_63-460delinsAT
XM_024446338.1:c.468-461_468-460delinsAT XP_024302106.1:n.468-461_468-460delinsAT
NM_006623.4:c.357-461_357-460delinsAT MANE Select NP_006614.2:n.357-461_357-460delinsAT