Canonical Allele Identifier: CA341851156

Gene: PHGDH

Linked Data

• MyVariant Identifiers: chr1:g.120279776G>C (hg19) ; chr1:g.119737153G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119737153G>C , CM000663.2:g.119737153G>C	GRCh38
NC_000001.10:g.120279776G>C , CM000663.1:g.120279776G>C	GRCh37
NC_000001.9:g.120081299G>C	NCBI36
NG_009188.1:g.30358G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.832G>C	ENSP00000358417.5:p.Val278Leu
ENST00000469443.2:n.652G>C
ENST00000641023.2:c.832G>C MANE Select	ENSP00000493175.1:p.Val278Leu
ENST00000641074.1:c.832G>C	ENSP00000493446.1:p.Val278Leu
ENST00000641115.1:c.832G>C	ENSP00000493264.1:p.Val278Leu
ENST00000641213.1:c.*485G>C	ENSP00000493079.1:n.*485G>C
ENST00000641314.1:n.817G>C
ENST00000641375.1:c.*668G>C	ENSP00000493089.1:n.*668G>C
ENST00000641597.1:c.832G>C	ENSP00000493382.1:p.Val278Leu
ENST00000641756.1:c.*576G>C	ENSP00000493147.1:n.*576G>C
ENST00000641811.1:c.588G>C
ENST00000641891.1:c.*658G>C	ENSP00000493288.1:n.*658G>C
ENST00000641927.1:n.772G>C
ENST00000641947.1:c.832G>C	ENSP00000492994.1:p.Val278Leu
ENST00000642021.1:n.954G>C
ENST00000369407.3:c.730G>C	ENSP00000358415.3:p.Val244Leu
ENST00000369409.8:c.832G>C	ENSP00000358417.4:p.Val278Leu
NM_006623.3:c.832G>C	NP_006614.2:p.Val278Leu
XM_011541226.1:c.1054G>C	XP_011539528.1:p.Val352Leu
XM_011541227.1:c.976G>C	XP_011539529.1:p.Val326Leu
XM_011541228.1:c.943G>C	XP_011539530.1:p.Val315Leu
XM_011541229.1:c.769G>C	XP_011539531.1:p.Val257Leu
XM_011541230.1:c.547G>C	XP_011539532.1:p.Val183Leu
XM_011541231.1:c.538G>C	XP_011539533.1:p.Val180Leu
XM_011541226.2:c.1054G>C	XP_011539528.1:p.Val352Leu
XM_011541227.2:c.976G>C	XP_011539529.1:p.Val326Leu
XM_011541228.2:c.943G>C	XP_011539530.1:p.Val315Leu
XM_011541231.2:c.538G>C	XP_011539533.1:p.Val180Leu
XM_024446338.1:c.943G>C	XP_024302106.1:p.Val315Leu
NM_006623.4:c.832G>C MANE Select	NP_006614.2:p.Val278Leu