Canonical Allele Identifier: CA1148731816

Gene: PHGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119726982_119726983delinsCC , CM000663.2:g.119726982_119726983delinsCC	GRCh38
NC_000001.10:g.120269605_120269606delinsCC , CM000663.1:g.120269605_120269606delinsCC	GRCh37
NC_000001.9:g.120071128_120071129delinsCC	NCBI36
NG_009188.1:g.20187_20188delinsCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.412-22_412-21delinsCC	ENSP00000358417.5:n.412-22_412-21delinsCC
ENST00000462324.2:n.495-22_495-21delinsCC
ENST00000641023.2:c.412-22_412-21delinsCC MANE Select	ENSP00000493175.1:n.412-22_412-21delinsCC
ENST00000641074.1:c.412-22_412-21delinsCC	ENSP00000493446.1:n.412-22_412-21delinsCC
ENST00000641115.1:c.412-22_412-21delinsCC	ENSP00000493264.1:n.412-22_412-21delinsCC
ENST00000641213.1:c.*65-22_*65-21delinsCC	ENSP00000493079.1:n.*65-22_*65-21delinsCC
ENST00000641247.1:c.*131-22_*131-21delinsCC	ENSP00000492955.1:n.*131-22_*131-21delinsCC
ENST00000641272.1:c.346-22_346-21delinsCC	ENSP00000493432.1:n.346-22_346-21delinsCC
ENST00000641314.1:n.397-22_397-21delinsCC
ENST00000641371.1:c.326-22_326-21delinsCC	ENSP00000493305.1:n.326-22_326-21delinsCC
ENST00000641375.1:c.*248-22_*248-21delinsCC	ENSP00000493089.1:n.*248-22_*248-21delinsCC
ENST00000641491.1:c.*65-22_*65-21delinsCC	ENSP00000493187.1:n.*65-22_*65-21delinsCC
ENST00000641570.1:c.*131-22_*131-21delinsCC	ENSP00000493213.1:n.*131-22_*131-21delinsCC
ENST00000641573.1:n.500-22_500-21delinsCC
ENST00000641587.1:c.*123-22_*123-21delinsCC	ENSP00000493453.1:n.*123-22_*123-21delinsCC
ENST00000641597.1:c.412-22_412-21delinsCC	ENSP00000493382.1:n.412-22_412-21delinsCC
ENST00000641711.1:n.636-22_636-21delinsCC
ENST00000641756.1:c.*156-22_*156-21delinsCC	ENSP00000493147.1:n.*156-22_*156-21delinsCC
ENST00000641811.1:c.168-22_168-21delinsCC
ENST00000641847.1:n.271-22_271-21delinsCC
ENST00000641891.1:c.*238-22_*238-21delinsCC	ENSP00000493288.1:n.*238-22_*238-21delinsCC
ENST00000641927.1:n.352-22_352-21delinsCC
ENST00000641947.1:c.412-22_412-21delinsCC	ENSP00000492994.1:n.412-22_412-21delinsCC
ENST00000642021.1:n.534-22_534-21delinsCC
ENST00000642041.1:c.*451-22_*451-21delinsCC	ENSP00000493415.1:n.*451-22_*451-21delinsCC
ENST00000369407.3:c.310-22_310-21delinsCC	ENSP00000358415.3:n.310-22_310-21delinsCC
ENST00000369409.8:c.412-22_412-21delinsCC	ENSP00000358417.4:n.412-22_412-21delinsCC
ENST00000462324.1:n.680-22_680-21delinsCC
ENST00000493622.5:n.601-22_601-21delinsCC
NM_006623.3:c.412-22_412-21delinsCC	NP_006614.2:n.412-22_412-21delinsCC
XM_011541226.1:c.634-22_634-21delinsCC	XP_011539528.1:n.634-22_634-21delinsCC
XM_011541227.1:c.556-22_556-21delinsCC	XP_011539529.1:n.556-22_556-21delinsCC
XM_011541228.1:c.523-22_523-21delinsCC	XP_011539530.1:n.523-22_523-21delinsCC
XM_011541229.1:c.349-22_349-21delinsCC	XP_011539531.1:n.349-22_349-21delinsCC
XM_011541230.1:c.127-22_127-21delinsCC	XP_011539532.1:n.127-22_127-21delinsCC
XM_011541231.1:c.118-22_118-21delinsCC	XP_011539533.1:n.118-22_118-21delinsCC
XM_011541226.2:c.634-22_634-21delinsCC	XP_011539528.1:n.634-22_634-21delinsCC
XM_011541227.2:c.556-22_556-21delinsCC	XP_011539529.1:n.556-22_556-21delinsCC
XM_011541228.2:c.523-22_523-21delinsCC	XP_011539530.1:n.523-22_523-21delinsCC
XM_011541231.2:c.118-22_118-21delinsCC	XP_011539533.1:n.118-22_118-21delinsCC
XM_024446338.1:c.523-22_523-21delinsCC	XP_024302106.1:n.523-22_523-21delinsCC
NM_006623.4:c.412-22_412-21delinsCC MANE Select	NP_006614.2:n.412-22_412-21delinsCC