Canonical Allele Identifier: CA1149143584

Gene: PHGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119737303_119737306delinsAGAG , CM000663.2:g.119737303_119737306delinsAGAG	GRCh38
NC_000001.10:g.120279926_120279929delinsAGAG , CM000663.1:g.120279926_120279929delinsAGAG	GRCh37
NC_000001.9:g.120081449_120081452delinsAGAG	NCBI36
NG_009188.1:g.30508_30511delinsAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.945+37_945+40delinsAGAG	ENSP00000358417.5:n.945+37_945+40delinsAGAG
ENST00000641023.2:c.945+37_945+40delinsAGAG MANE Select	ENSP00000493175.1:n.945+37_945+40delinsAGAG
ENST00000641074.1:c.945+37_945+40delinsAGAG	ENSP00000493446.1:n.945+37_945+40delinsAGAG
ENST00000641115.1:c.945+37_945+40delinsAGAG	ENSP00000493264.1:n.945+37_945+40delinsAGAG
ENST00000641213.1:c.*598+37_*598+40delinsAGAG	ENSP00000493079.1:n.*598+37_*598+40delinsAGAG
ENST00000641314.1:n.930+37_930+40delinsAGAG
ENST00000641375.1:c.*781+37_*781+40delinsAGAG	ENSP00000493089.1:n.*781+37_*781+40delinsAGAG
ENST00000641597.1:c.945+37_945+40delinsAGAG	ENSP00000493382.1:n.945+37_945+40delinsAGAG
ENST00000641756.1:c.*689+37_*689+40delinsAGAG	ENSP00000493147.1:n.*689+37_*689+40delinsAGAG
ENST00000641811.1:c.701+37_701+40delinsAGAG
ENST00000641891.1:c.*771+37_*771+40delinsAGAG	ENSP00000493288.1:n.*771+37_*771+40delinsAGAG
ENST00000641927.1:n.885+37_885+40delinsAGAG
ENST00000641939.1:n.48+37_48+40delinsAGAG
ENST00000641947.1:c.945+37_945+40delinsAGAG	ENSP00000492994.1:n.945+37_945+40delinsAGAG
ENST00000642021.1:n.1067+37_1067+40delinsAGAG
ENST00000369407.3:c.843+37_843+40delinsAGAG	ENSP00000358415.3:n.843+37_843+40delinsAGAG
ENST00000369409.8:c.945+37_945+40delinsAGAG	ENSP00000358417.4:n.945+37_945+40delinsAGAG
NM_006623.3:c.945+37_945+40delinsAGAG	NP_006614.2:n.945+37_945+40delinsAGAG
XM_011541226.1:c.1167+37_1167+40delinsAGAG	XP_011539528.1:n.1167+37_1167+40delinsAGAG
XM_011541227.1:c.1089+37_1089+40delinsAGAG	XP_011539529.1:n.1089+37_1089+40delinsAGAG
XM_011541228.1:c.1056+37_1056+40delinsAGAG	XP_011539530.1:n.1056+37_1056+40delinsAGAG
XM_011541229.1:c.882+37_882+40delinsAGAG	XP_011539531.1:n.882+37_882+40delinsAGAG
XM_011541230.1:c.660+37_660+40delinsAGAG	XP_011539532.1:n.660+37_660+40delinsAGAG
XM_011541231.1:c.651+37_651+40delinsAGAG	XP_011539533.1:n.651+37_651+40delinsAGAG
XM_011541226.2:c.1167+37_1167+40delinsAGAG	XP_011539528.1:n.1167+37_1167+40delinsAGAG
XM_011541227.2:c.1089+37_1089+40delinsAGAG	XP_011539529.1:n.1089+37_1089+40delinsAGAG
XM_011541228.2:c.1056+37_1056+40delinsAGAG	XP_011539530.1:n.1056+37_1056+40delinsAGAG
XM_011541231.2:c.651+37_651+40delinsAGAG	XP_011539533.1:n.651+37_651+40delinsAGAG
XM_024446338.1:c.1056+37_1056+40delinsAGAG	XP_024302106.1:n.1056+37_1056+40delinsAGAG
NM_006623.4:c.945+37_945+40delinsAGAG MANE Select	NP_006614.2:n.945+37_945+40delinsAGAG