Canonical Allele Identifier: CA1192431799

Gene: PHGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119727000G= , CM000663.2:g.119727000G=	GRCh38
NC_000001.10:g.120269623G= , CM000663.1:g.120269623G=	GRCh37
NC_000001.9:g.120071146G=	NCBI36
NG_009188.1:g.20205G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.412-4G=	ENSP00000358417.5:n.412-4G=
ENST00000462324.2:n.495-4G=
ENST00000641023.2:c.412-4G= MANE Select	ENSP00000493175.1:n.412-4G=
ENST00000641074.1:c.412-4G=	ENSP00000493446.1:n.412-4G=
ENST00000641115.1:c.412-4G=	ENSP00000493264.1:n.412-4G=
ENST00000641213.1:c.*65-4G=	ENSP00000493079.1:n.*65-4G=
ENST00000641247.1:c.*131-4G=	ENSP00000492955.1:n.*131-4G=
ENST00000641272.1:c.346-4G=	ENSP00000493432.1:n.346-4G=
ENST00000641314.1:n.397-4G=
ENST00000641371.1:c.326-4G=	ENSP00000493305.1:n.326-4G=
ENST00000641375.1:c.*248-4G=	ENSP00000493089.1:n.*248-4G=
ENST00000641491.1:c.*65-4G=	ENSP00000493187.1:n.*65-4G=
ENST00000641570.1:c.*131-4G=	ENSP00000493213.1:n.*131-4G=
ENST00000641573.1:n.500-4G=
ENST00000641587.1:c.*123-4G=	ENSP00000493453.1:n.*123-4G=
ENST00000641597.1:c.412-4G=	ENSP00000493382.1:n.412-4G=
ENST00000641711.1:n.636-4G=
ENST00000641756.1:c.*156-4G=	ENSP00000493147.1:n.*156-4G=
ENST00000641811.1:c.168-4G=
ENST00000641847.1:n.271-4G=
ENST00000641891.1:c.*238-4G=	ENSP00000493288.1:n.*238-4G=
ENST00000641927.1:n.352-4G=
ENST00000641947.1:c.412-4G=	ENSP00000492994.1:n.412-4G=
ENST00000642021.1:n.534-4G=
ENST00000642041.1:c.*451-4G=	ENSP00000493415.1:n.*451-4G=
ENST00000369407.3:c.310-4G=	ENSP00000358415.3:n.310-4G=
ENST00000369409.8:c.412-4G=	ENSP00000358417.4:n.412-4G=
ENST00000462324.1:n.680-4G=
ENST00000493622.5:n.601-4G=
NM_006623.3:c.412-4G=	NP_006614.2:n.412-4G=
XM_011541226.1:c.634-4G=	XP_011539528.1:n.634-4G=
XM_011541227.1:c.556-4G=	XP_011539529.1:n.556-4G=
XM_011541228.1:c.523-4G=	XP_011539530.1:n.523-4G=
XM_011541229.1:c.349-4G=	XP_011539531.1:n.349-4G=
XM_011541230.1:c.127-4G=	XP_011539532.1:n.127-4G=
XM_011541231.1:c.118-4G=	XP_011539533.1:n.118-4G=
XM_011541226.2:c.634-4G=	XP_011539528.1:n.634-4G=
XM_011541227.2:c.556-4G=	XP_011539529.1:n.556-4G=
XM_011541228.2:c.523-4G=	XP_011539530.1:n.523-4G=
XM_011541231.2:c.118-4G=	XP_011539533.1:n.118-4G=
XM_024446338.1:c.523-4G=	XP_024302106.1:n.523-4G=
NM_006623.4:c.412-4G= MANE Select	NP_006614.2:n.412-4G=