Canonical Allele Identifier: CA420013945

Gene: PHGDH

Linked Data

• ClinVar Variation Id: 1356295
• ClinVar RCV Id: RCV001870015
• dbSNP Id: rs1297161098
• gnomAD v2: 1-120279796-G-T
• MyVariant Identifiers: chr1:g.120279796G>T (hg19) ; chr1:g.119737173G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119737173G>T , CM000663.2:g.119737173G>T	GRCh38
NC_000001.10:g.120279796G>T , CM000663.1:g.120279796G>T	GRCh37
NC_000001.9:g.120081319G>T	NCBI36
NG_009188.1:g.30378G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.852G>T	ENSP00000358417.5:p.Leu284=
ENST00000641023.2:c.852G>T MANE Select	ENSP00000493175.1:p.Leu284=
ENST00000641074.1:c.852G>T	ENSP00000493446.1:p.Leu284=
ENST00000641115.1:c.852G>T	ENSP00000493264.1:p.Leu284=
ENST00000641213.1:c.*505G>T	ENSP00000493079.1:n.*505G>T
ENST00000641314.1:n.837G>T
ENST00000641375.1:c.*688G>T	ENSP00000493089.1:n.*688G>T
ENST00000641597.1:c.852G>T	ENSP00000493382.1:p.Leu284=
ENST00000641756.1:c.*596G>T	ENSP00000493147.1:n.*596G>T
ENST00000641811.1:c.608G>T
ENST00000641891.1:c.*678G>T	ENSP00000493288.1:n.*678G>T
ENST00000641927.1:n.792G>T
ENST00000641947.1:c.852G>T	ENSP00000492994.1:p.Leu284=
ENST00000642021.1:n.974G>T
ENST00000369407.3:c.750G>T	ENSP00000358415.3:p.Leu250=
ENST00000369409.8:c.852G>T	ENSP00000358417.4:p.Leu284=
NM_006623.3:c.852G>T	NP_006614.2:p.Leu284=
XM_011541226.1:c.1074G>T	XP_011539528.1:p.Leu358=
XM_011541227.1:c.996G>T	XP_011539529.1:p.Leu332=
XM_011541228.1:c.963G>T	XP_011539530.1:p.Leu321=
XM_011541229.1:c.789G>T	XP_011539531.1:p.Leu263=
XM_011541230.1:c.567G>T	XP_011539532.1:p.Leu189=
XM_011541231.1:c.558G>T	XP_011539533.1:p.Leu186=
XM_011541226.2:c.1074G>T	XP_011539528.1:p.Leu358=
XM_011541227.2:c.996G>T	XP_011539529.1:p.Leu332=
XM_011541228.2:c.963G>T	XP_011539530.1:p.Leu321=
XM_011541231.2:c.558G>T	XP_011539533.1:p.Leu186=
XM_024446338.1:c.963G>T	XP_024302106.1:p.Leu321=
NM_006623.4:c.852G>T MANE Select	NP_006614.2:p.Leu284=