Canonical Allele Identifier: CA1192434142

Gene: PHGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119737132G= , CM000663.2:g.119737132G=	GRCh38
NC_000001.10:g.120279755G= , CM000663.1:g.120279755G=	GRCh37
NC_000001.9:g.120081278G=	NCBI36
NG_009188.1:g.30337G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.811G=	ENSP00000358417.5:p.Ala271=
ENST00000469443.2:n.631G=
ENST00000641023.2:c.811G= MANE Select	ENSP00000493175.1:p.Ala271=
ENST00000641074.1:c.811G=	ENSP00000493446.1:p.Ala271=
ENST00000641115.1:c.811G=	ENSP00000493264.1:p.Ala271=
ENST00000641213.1:c.*464G=	ENSP00000493079.1:n.*464G=
ENST00000641314.1:n.796G=
ENST00000641375.1:c.*647G=	ENSP00000493089.1:n.*647G=
ENST00000641597.1:c.811G=	ENSP00000493382.1:p.Ala271=
ENST00000641756.1:c.*555G=	ENSP00000493147.1:n.*555G=
ENST00000641811.1:c.567G=
ENST00000641891.1:c.*637G=	ENSP00000493288.1:n.*637G=
ENST00000641927.1:n.751G=
ENST00000641947.1:c.811G=	ENSP00000492994.1:p.Ala271=
ENST00000642021.1:n.933G=
ENST00000369407.3:c.709G=	ENSP00000358415.3:p.Ala237=
ENST00000369409.8:c.811G=	ENSP00000358417.4:p.Ala271=
NM_006623.3:c.811G=	NP_006614.2:p.Ala271=
XM_011541226.1:c.1033G=	XP_011539528.1:p.Ala345=
XM_011541227.1:c.955G=	XP_011539529.1:p.Ala319=
XM_011541228.1:c.922G=	XP_011539530.1:p.Ala308=
XM_011541229.1:c.748G=	XP_011539531.1:p.Ala250=
XM_011541230.1:c.526G=	XP_011539532.1:p.Ala176=
XM_011541231.1:c.517G=	XP_011539533.1:p.Ala173=
XM_011541226.2:c.1033G=	XP_011539528.1:p.Ala345=
XM_011541227.2:c.955G=	XP_011539529.1:p.Ala319=
XM_011541228.2:c.922G=	XP_011539530.1:p.Ala308=
XM_011541231.2:c.517G=	XP_011539533.1:p.Ala173=
XM_024446338.1:c.922G=	XP_024302106.1:p.Ala308=
NM_006623.4:c.811G= MANE Select	NP_006614.2:p.Ala271=