Canonical Allele Identifier: CA1192434109

Gene: PHGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119737100_119737104delinsCTCTT , CM000663.2:g.119737100_119737104delinsCTCTT	GRCh38
NC_000001.10:g.120279723_120279727delinsCTCTT , CM000663.1:g.120279723_120279727delinsCTCTT	GRCh37
NC_000001.9:g.120081246_120081250delinsCTCTT	NCBI36
NG_009188.1:g.30305_30309delinsCTCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000369409.9:c.793-14_793-10delinsCTCTT	ENSP00000358417.5:n.793-14_793-10delinsCTCTT
ENST00000469443.2:n.613-14_613-10delinsCTCTT
ENST00000641023.2:c.793-14_793-10delinsCTCTT MANE Select	ENSP00000493175.1:n.793-14_793-10delinsCTCTT
ENST00000641074.1:c.793-14_793-10delinsCTCTT	ENSP00000493446.1:n.793-14_793-10delinsCTCTT
ENST00000641115.1:c.793-14_793-10delinsCTCTT	ENSP00000493264.1:n.793-14_793-10delinsCTCTT
ENST00000641213.1:c.*446-14_*446-10delinsCTCTT	ENSP00000493079.1:n.*446-14_*446-10delinsCTCTT
ENST00000641314.1:n.778-14_778-10delinsCTCTT
ENST00000641375.1:c.*629-14_*629-10delinsCTCTT	ENSP00000493089.1:n.*629-14_*629-10delinsCTCTT
ENST00000641597.1:c.793-14_793-10delinsCTCTT	ENSP00000493382.1:n.793-14_793-10delinsCTCTT
ENST00000641756.1:c.*537-14_*537-10delinsCTCTT	ENSP00000493147.1:n.*537-14_*537-10delinsCTCTT
ENST00000641811.1:c.549-14_549-10delinsCTCTT
ENST00000641891.1:c.*619-14_*619-10delinsCTCTT	ENSP00000493288.1:n.*619-14_*619-10delinsCTCTT
ENST00000641927.1:n.733-14_733-10delinsCTCTT
ENST00000641947.1:c.793-14_793-10delinsCTCTT	ENSP00000492994.1:n.793-14_793-10delinsCTCTT
ENST00000642021.1:n.915-14_915-10delinsCTCTT
ENST00000369407.3:c.691-14_691-10delinsCTCTT	ENSP00000358415.3:n.691-14_691-10delinsCTCTT
ENST00000369409.8:c.793-14_793-10delinsCTCTT	ENSP00000358417.4:n.793-14_793-10delinsCTCTT
NM_006623.3:c.793-14_793-10delinsCTCTT	NP_006614.2:n.793-14_793-10delinsCTCTT
XM_011541226.1:c.1015-14_1015-10delinsCTCTT	XP_011539528.1:n.1015-14_1015-10delinsCTCTT
XM_011541227.1:c.937-14_937-10delinsCTCTT	XP_011539529.1:n.937-14_937-10delinsCTCTT
XM_011541228.1:c.904-14_904-10delinsCTCTT	XP_011539530.1:n.904-14_904-10delinsCTCTT
XM_011541229.1:c.730-14_730-10delinsCTCTT	XP_011539531.1:n.730-14_730-10delinsCTCTT
XM_011541230.1:c.508-14_508-10delinsCTCTT	XP_011539532.1:n.508-14_508-10delinsCTCTT
XM_011541231.1:c.499-14_499-10delinsCTCTT	XP_011539533.1:n.499-14_499-10delinsCTCTT
XM_011541226.2:c.1015-14_1015-10delinsCTCTT	XP_011539528.1:n.1015-14_1015-10delinsCTCTT
XM_011541227.2:c.937-14_937-10delinsCTCTT	XP_011539529.1:n.937-14_937-10delinsCTCTT
XM_011541228.2:c.904-14_904-10delinsCTCTT	XP_011539530.1:n.904-14_904-10delinsCTCTT
XM_011541231.2:c.499-14_499-10delinsCTCTT	XP_011539533.1:n.499-14_499-10delinsCTCTT
XM_024446338.1:c.904-14_904-10delinsCTCTT	XP_024302106.1:n.904-14_904-10delinsCTCTT
NM_006623.4:c.793-14_793-10delinsCTCTT MANE Select	NP_006614.2:n.793-14_793-10delinsCTCTT