Canonical Allele Identifier: CA1192434172

Gene: PHGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119737179C= , CM000663.2:g.119737179C=	GRCh38
NC_000001.10:g.120279802C= , CM000663.1:g.120279802C=	GRCh37
NC_000001.9:g.120081325C=	NCBI36
NG_009188.1:g.30384C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.858C=	ENSP00000358417.5:p.Ala286=
ENST00000641023.2:c.858C= MANE Select	ENSP00000493175.1:p.Ala286=
ENST00000641074.1:c.858C=	ENSP00000493446.1:p.Ala286=
ENST00000641115.1:c.858C=	ENSP00000493264.1:p.Ala286=
ENST00000641213.1:c.*511C=	ENSP00000493079.1:n.*511C=
ENST00000641314.1:n.843C=
ENST00000641375.1:c.*694C=	ENSP00000493089.1:n.*694C=
ENST00000641597.1:c.858C=	ENSP00000493382.1:p.Ala286=
ENST00000641756.1:c.*602C=	ENSP00000493147.1:n.*602C=
ENST00000641811.1:c.614C=
ENST00000641891.1:c.*684C=	ENSP00000493288.1:n.*684C=
ENST00000641927.1:n.798C=
ENST00000641947.1:c.858C=	ENSP00000492994.1:p.Ala286=
ENST00000642021.1:n.980C=
ENST00000369407.3:c.756C=	ENSP00000358415.3:p.Ala252=
ENST00000369409.8:c.858C=	ENSP00000358417.4:p.Ala286=
NM_006623.3:c.858C=	NP_006614.2:p.Ala286=
XM_011541226.1:c.1080C=	XP_011539528.1:p.Ala360=
XM_011541227.1:c.1002C=	XP_011539529.1:p.Ala334=
XM_011541228.1:c.969C=	XP_011539530.1:p.Ala323=
XM_011541229.1:c.795C=	XP_011539531.1:p.Ala265=
XM_011541230.1:c.573C=	XP_011539532.1:p.Ala191=
XM_011541231.1:c.564C=	XP_011539533.1:p.Ala188=
XM_011541226.2:c.1080C=	XP_011539528.1:p.Ala360=
XM_011541227.2:c.1002C=	XP_011539529.1:p.Ala334=
XM_011541228.2:c.969C=	XP_011539530.1:p.Ala323=
XM_011541231.2:c.564C=	XP_011539533.1:p.Ala188=
XM_024446338.1:c.969C=	XP_024302106.1:p.Ala323=
NM_006623.4:c.858C= MANE Select	NP_006614.2:p.Ala286=