Canonical Allele Identifier: CA1192434159

Gene: PHGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119737167C= , CM000663.2:g.119737167C=	GRCh38
NC_000001.10:g.120279790C= , CM000663.1:g.120279790C=	GRCh37
NC_000001.9:g.120081313C=	NCBI36
NG_009188.1:g.30372C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.846C=	ENSP00000358417.5:p.Pro282=
ENST00000641023.2:c.846C= MANE Select	ENSP00000493175.1:p.Pro282=
ENST00000641074.1:c.846C=	ENSP00000493446.1:p.Pro282=
ENST00000641115.1:c.846C=	ENSP00000493264.1:p.Pro282=
ENST00000641213.1:c.*499C=	ENSP00000493079.1:n.*499C=
ENST00000641314.1:n.831C=
ENST00000641375.1:c.*682C=	ENSP00000493089.1:n.*682C=
ENST00000641597.1:c.846C=	ENSP00000493382.1:p.Pro282=
ENST00000641756.1:c.*590C=	ENSP00000493147.1:n.*590C=
ENST00000641811.1:c.602C=
ENST00000641891.1:c.*672C=	ENSP00000493288.1:n.*672C=
ENST00000641927.1:n.786C=
ENST00000641947.1:c.846C=	ENSP00000492994.1:p.Pro282=
ENST00000642021.1:n.968C=
ENST00000369407.3:c.744C=	ENSP00000358415.3:p.Pro248=
ENST00000369409.8:c.846C=	ENSP00000358417.4:p.Pro282=
NM_006623.3:c.846C=	NP_006614.2:p.Pro282=
XM_011541226.1:c.1068C=	XP_011539528.1:p.Pro356=
XM_011541227.1:c.990C=	XP_011539529.1:p.Pro330=
XM_011541228.1:c.957C=	XP_011539530.1:p.Pro319=
XM_011541229.1:c.783C=	XP_011539531.1:p.Pro261=
XM_011541230.1:c.561C=	XP_011539532.1:p.Pro187=
XM_011541231.1:c.552C=	XP_011539533.1:p.Pro184=
XM_011541226.2:c.1068C=	XP_011539528.1:p.Pro356=
XM_011541227.2:c.990C=	XP_011539529.1:p.Pro330=
XM_011541228.2:c.957C=	XP_011539530.1:p.Pro319=
XM_011541231.2:c.552C=	XP_011539533.1:p.Pro184=
XM_024446338.1:c.957C=	XP_024302106.1:p.Pro319=
NM_006623.4:c.846C= MANE Select	NP_006614.2:p.Pro282=