Canonical Allele Identifier: CA1192434368

Gene: PHGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119737452_119737467delinsTAGCAGAGGCCTTGGC , CM000663.2:g.119737452_119737467delinsTAGCAGAGGCCTTGGC	GRCh38
NC_000001.10:g.120280075_120280090delinsTAGCAGAGGCCTTGGC , CM000663.1:g.120280075_120280090delinsTAGCAGAGGCCTTGGC	GRCh37
NC_000001.9:g.120081598_120081613delinsTAGCAGAGGCCTTGGC	NCBI36
NG_009188.1:g.30657_30672delinsTAGCAGAGGCCTTGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.945+186_945+201delinsTAGCAGAGGCCTTGGC	ENSP00000358417.5:n.945+186_945+201delinsTAGCAGAGGCCTTGGC
ENST00000641023.2:c.945+186_945+201delinsTAGCAGAGGCCTTGGC MANE Select	ENSP00000493175.1:n.945+186_945+201delinsTAGCAGAGGCCTTGGC
ENST00000641074.1:c.945+186_945+201delinsTAGCAGAGGCCTTGGC	ENSP00000493446.1:n.945+186_945+201delinsTAGCAGAGGCCTTGGC
ENST00000641115.1:c.945+186_945+201delinsTAGCAGAGGCCTTGGC	ENSP00000493264.1:n.945+186_945+201delinsTAGCAGAGGCCTTGGC
ENST00000641213.1:c.*598+186_*598+201delinsTAGCAGAGGCCTTGGC	ENSP00000493079.1:n.*598+186_*598+201delinsTAGCAGAGGCCTTGGC
ENST00000641314.1:n.930+186_930+201delinsTAGCAGAGGCCTTGGC
ENST00000641375.1:c.*781+186_*781+201delinsTAGCAGAGGCCTTGGC	ENSP00000493089.1:n.*781+186_*781+201delinsTAGCAGAGGCCTTGGC
ENST00000641597.1:c.945+186_945+201delinsTAGCAGAGGCCTTGGC	ENSP00000493382.1:n.945+186_945+201delinsTAGCAGAGGCCTTGGC
ENST00000641756.1:c.*689+186_*689+201delinsTAGCAGAGGCCTTGGC	ENSP00000493147.1:n.*689+186_*689+201delinsTAGCAGAGGCCTTGGC
ENST00000641811.1:c.701+186_701+201delinsTAGCAGAGGCCTTGGC
ENST00000641891.1:c.*771+186_*771+201delinsTAGCAGAGGCCTTGGC	ENSP00000493288.1:n.*771+186_*771+201delinsTAGCAGAGGCCTTGGC
ENST00000641927.1:n.885+186_885+201delinsTAGCAGAGGCCTTGGC
ENST00000641939.1:n.48+186_48+201delinsTAGCAGAGGCCTTGGC
ENST00000641947.1:c.945+186_945+201delinsTAGCAGAGGCCTTGGC	ENSP00000492994.1:n.945+186_945+201delinsTAGCAGAGGCCTTGGC
ENST00000642021.1:n.1067+186_1067+201delinsTAGCAGAGGCCTTGGC
ENST00000369407.3:c.843+186_843+201delinsTAGCAGAGGCCTTGGC	ENSP00000358415.3:n.843+186_843+201delinsTAGCAGAGGCCTTGGC
ENST00000369409.8:c.945+186_945+201delinsTAGCAGAGGCCTTGGC	ENSP00000358417.4:n.945+186_945+201delinsTAGCAGAGGCCTTGGC
NM_006623.3:c.945+186_945+201delinsTAGCAGAGGCCTTGGC	NP_006614.2:n.945+186_945+201delinsTAGCAGAGGCCTTGGC
XM_011541226.1:c.1167+186_1167+201delinsTAGCAGAGGCCTTGGC	XP_011539528.1:n.1167+186_1167+201delinsTAGCAGAGGCCTTGGC
XM_011541227.1:c.1089+186_1089+201delinsTAGCAGAGGCCTTGGC	XP_011539529.1:n.1089+186_1089+201delinsTAGCAGAGGCCTTGGC
XM_011541228.1:c.1056+186_1056+201delinsTAGCAGAGGCCTTGGC	XP_011539530.1:n.1056+186_1056+201delinsTAGCAGAGGCCTTGGC
XM_011541229.1:c.882+186_882+201delinsTAGCAGAGGCCTTGGC	XP_011539531.1:n.882+186_882+201delinsTAGCAGAGGCCTTGGC
XM_011541230.1:c.660+186_660+201delinsTAGCAGAGGCCTTGGC	XP_011539532.1:n.660+186_660+201delinsTAGCAGAGGCCTTGGC
XM_011541231.1:c.651+186_651+201delinsTAGCAGAGGCCTTGGC	XP_011539533.1:n.651+186_651+201delinsTAGCAGAGGCCTTGGC
XM_011541226.2:c.1167+186_1167+201delinsTAGCAGAGGCCTTGGC	XP_011539528.1:n.1167+186_1167+201delinsTAGCAGAGGCCTTGGC
XM_011541227.2:c.1089+186_1089+201delinsTAGCAGAGGCCTTGGC	XP_011539529.1:n.1089+186_1089+201delinsTAGCAGAGGCCTTGGC
XM_011541228.2:c.1056+186_1056+201delinsTAGCAGAGGCCTTGGC	XP_011539530.1:n.1056+186_1056+201delinsTAGCAGAGGCCTTGGC
XM_011541231.2:c.651+186_651+201delinsTAGCAGAGGCCTTGGC	XP_011539533.1:n.651+186_651+201delinsTAGCAGAGGCCTTGGC
XM_024446338.1:c.1056+186_1056+201delinsTAGCAGAGGCCTTGGC	XP_024302106.1:n.1056+186_1056+201delinsTAGCAGAGGCCTTGGC
NM_006623.4:c.945+186_945+201delinsTAGCAGAGGCCTTGGC MANE Select	NP_006614.2:n.945+186_945+201delinsTAGCAGAGGCCTTGGC