Canonical Allele Identifier: CA1192434125

Gene: PHGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119737118C= , CM000663.2:g.119737118C=	GRCh38
NC_000001.10:g.120279741C= , CM000663.1:g.120279741C=	GRCh37
NC_000001.9:g.120081264C=	NCBI36
NG_009188.1:g.30323C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.797C=	ENSP00000358417.5:p.Pro266=
ENST00000469443.2:n.617C=
ENST00000641023.2:c.797C= MANE Select	ENSP00000493175.1:p.Pro266=
ENST00000641074.1:c.797C=	ENSP00000493446.1:p.Pro266=
ENST00000641115.1:c.797C=	ENSP00000493264.1:p.Pro266=
ENST00000641213.1:c.*450C=	ENSP00000493079.1:n.*450C=
ENST00000641314.1:n.782C=
ENST00000641375.1:c.*633C=	ENSP00000493089.1:n.*633C=
ENST00000641597.1:c.797C=	ENSP00000493382.1:p.Pro266=
ENST00000641756.1:c.*541C=	ENSP00000493147.1:n.*541C=
ENST00000641811.1:c.553C=
ENST00000641891.1:c.*623C=	ENSP00000493288.1:n.*623C=
ENST00000641927.1:n.737C=
ENST00000641947.1:c.797C=	ENSP00000492994.1:p.Pro266=
ENST00000642021.1:n.919C=
ENST00000369407.3:c.695C=	ENSP00000358415.3:p.Pro232=
ENST00000369409.8:c.797C=	ENSP00000358417.4:p.Pro266=
NM_006623.3:c.797C=	NP_006614.2:p.Pro266=
XM_011541226.1:c.1019C=	XP_011539528.1:p.Pro340=
XM_011541227.1:c.941C=	XP_011539529.1:p.Pro314=
XM_011541228.1:c.908C=	XP_011539530.1:p.Pro303=
XM_011541229.1:c.734C=	XP_011539531.1:p.Pro245=
XM_011541230.1:c.512C=	XP_011539532.1:p.Pro171=
XM_011541231.1:c.503C=	XP_011539533.1:p.Pro168=
XM_011541226.2:c.1019C=	XP_011539528.1:p.Pro340=
XM_011541227.2:c.941C=	XP_011539529.1:p.Pro314=
XM_011541228.2:c.908C=	XP_011539530.1:p.Pro303=
XM_011541231.2:c.503C=	XP_011539533.1:p.Pro168=
XM_024446338.1:c.908C=	XP_024302106.1:p.Pro303=
NM_006623.4:c.797C= MANE Select	NP_006614.2:p.Pro266=