Canonical Allele Identifier: CA886278657

Gene: PHGDH

Linked Data

• dbSNP Id: rs1261800491
• gnomAD v3: 1-119726447-T-C
• gnomAD v4: 1-119726447-T-C
• MyVariant Identifiers: chr1:g.120269070T>C (hg19) ; chr1:g.119726447T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119726447T>C , CM000663.2:g.119726447T>C	GRCh38
NC_000001.10:g.120269070T>C , CM000663.1:g.120269070T>C	GRCh37
NC_000001.9:g.120070593T>C	NCBI36
NG_009188.1:g.19652T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.357-404T>C	ENSP00000358417.5:n.357-404T>C
ENST00000462324.2:n.440-404T>C
ENST00000641023.2:c.357-404T>C MANE Select	ENSP00000493175.1:n.357-404T>C
ENST00000641074.1:c.357-404T>C	ENSP00000493446.1:n.357-404T>C
ENST00000641115.1:c.357-404T>C	ENSP00000493264.1:n.357-404T>C
ENST00000641213.1:c.*10-404T>C	ENSP00000493079.1:n.*10-404T>C
ENST00000641247.1:c.*76-404T>C	ENSP00000492955.1:n.*76-404T>C
ENST00000641272.1:c.291-404T>C	ENSP00000493432.1:n.291-404T>C
ENST00000641314.1:n.342-404T>C
ENST00000641371.1:c.271-404T>C	ENSP00000493305.1:n.271-404T>C
ENST00000641375.1:c.*193-404T>C	ENSP00000493089.1:n.*193-404T>C
ENST00000641491.1:c.*10-404T>C	ENSP00000493187.1:n.*10-404T>C
ENST00000641513.1:c.*101-404T>C	ENSP00000493398.1:n.*101-404T>C
ENST00000641570.1:c.*76-404T>C	ENSP00000493213.1:n.*76-404T>C
ENST00000641573.1:n.445-404T>C
ENST00000641587.1:c.*68-404T>C	ENSP00000493453.1:n.*68-404T>C
ENST00000641597.1:c.357-404T>C	ENSP00000493382.1:n.357-404T>C
ENST00000641711.1:n.581-404T>C
ENST00000641756.1:c.*101-404T>C	ENSP00000493147.1:n.*101-404T>C
ENST00000641811.1:c.113-404T>C
ENST00000641891.1:c.*183-404T>C	ENSP00000493288.1:n.*183-404T>C
ENST00000641927.1:n.297-404T>C
ENST00000641947.1:c.357-404T>C	ENSP00000492994.1:n.357-404T>C
ENST00000642021.1:n.479-404T>C
ENST00000642041.1:c.*396-404T>C	ENSP00000493415.1:n.*396-404T>C
ENST00000369407.3:c.255-404T>C	ENSP00000358415.3:n.255-404T>C
ENST00000369409.8:c.357-404T>C	ENSP00000358417.4:n.357-404T>C
ENST00000462324.1:n.625-404T>C
ENST00000493622.5:n.546-404T>C
NM_006623.3:c.357-404T>C	NP_006614.2:n.357-404T>C
XM_011541226.1:c.579-404T>C	XP_011539528.1:n.579-404T>C
XM_011541227.1:c.501-404T>C	XP_011539529.1:n.501-404T>C
XM_011541228.1:c.468-404T>C	XP_011539530.1:n.468-404T>C
XM_011541229.1:c.294-404T>C	XP_011539531.1:n.294-404T>C
XM_011541230.1:c.72-404T>C	XP_011539532.1:n.72-404T>C
XM_011541231.1:c.63-404T>C	XP_011539533.1:n.63-404T>C
XM_011541226.2:c.579-404T>C	XP_011539528.1:n.579-404T>C
XM_011541227.2:c.501-404T>C	XP_011539529.1:n.501-404T>C
XM_011541228.2:c.468-404T>C	XP_011539530.1:n.468-404T>C
XM_011541231.2:c.63-404T>C	XP_011539533.1:n.63-404T>C
XM_024446338.1:c.468-404T>C	XP_024302106.1:n.468-404T>C
NM_006623.4:c.357-404T>C MANE Select	NP_006614.2:n.357-404T>C