Canonical Allele Identifier: CA1192434254

Gene: PHGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119737305_119737306delinsAG , CM000663.2:g.119737305_119737306delinsAG	GRCh38
NC_000001.10:g.120279928_120279929delinsAG , CM000663.1:g.120279928_120279929delinsAG	GRCh37
NC_000001.9:g.120081451_120081452delinsAG	NCBI36
NG_009188.1:g.30510_30511delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.945+39_945+40delinsAG	ENSP00000358417.5:n.945+39_945+40delinsAG
ENST00000641023.2:c.945+39_945+40delinsAG MANE Select	ENSP00000493175.1:n.945+39_945+40delinsAG
ENST00000641074.1:c.945+39_945+40delinsAG	ENSP00000493446.1:n.945+39_945+40delinsAG
ENST00000641115.1:c.945+39_945+40delinsAG	ENSP00000493264.1:n.945+39_945+40delinsAG
ENST00000641213.1:c.*598+39_*598+40delinsAG	ENSP00000493079.1:n.*598+39_*598+40delinsAG
ENST00000641314.1:n.930+39_930+40delinsAG
ENST00000641375.1:c.*781+39_*781+40delinsAG	ENSP00000493089.1:n.*781+39_*781+40delinsAG
ENST00000641597.1:c.945+39_945+40delinsAG	ENSP00000493382.1:n.945+39_945+40delinsAG
ENST00000641756.1:c.*689+39_*689+40delinsAG	ENSP00000493147.1:n.*689+39_*689+40delinsAG
ENST00000641811.1:c.701+39_701+40delinsAG
ENST00000641891.1:c.*771+39_*771+40delinsAG	ENSP00000493288.1:n.*771+39_*771+40delinsAG
ENST00000641927.1:n.885+39_885+40delinsAG
ENST00000641939.1:n.48+39_48+40delinsAG
ENST00000641947.1:c.945+39_945+40delinsAG	ENSP00000492994.1:n.945+39_945+40delinsAG
ENST00000642021.1:n.1067+39_1067+40delinsAG
ENST00000369407.3:c.843+39_843+40delinsAG	ENSP00000358415.3:n.843+39_843+40delinsAG
ENST00000369409.8:c.945+39_945+40delinsAG	ENSP00000358417.4:n.945+39_945+40delinsAG
NM_006623.3:c.945+39_945+40delinsAG	NP_006614.2:n.945+39_945+40delinsAG
XM_011541226.1:c.1167+39_1167+40delinsAG	XP_011539528.1:n.1167+39_1167+40delinsAG
XM_011541227.1:c.1089+39_1089+40delinsAG	XP_011539529.1:n.1089+39_1089+40delinsAG
XM_011541228.1:c.1056+39_1056+40delinsAG	XP_011539530.1:n.1056+39_1056+40delinsAG
XM_011541229.1:c.882+39_882+40delinsAG	XP_011539531.1:n.882+39_882+40delinsAG
XM_011541230.1:c.660+39_660+40delinsAG	XP_011539532.1:n.660+39_660+40delinsAG
XM_011541231.1:c.651+39_651+40delinsAG	XP_011539533.1:n.651+39_651+40delinsAG
XM_011541226.2:c.1167+39_1167+40delinsAG	XP_011539528.1:n.1167+39_1167+40delinsAG
XM_011541227.2:c.1089+39_1089+40delinsAG	XP_011539529.1:n.1089+39_1089+40delinsAG
XM_011541228.2:c.1056+39_1056+40delinsAG	XP_011539530.1:n.1056+39_1056+40delinsAG
XM_011541231.2:c.651+39_651+40delinsAG	XP_011539533.1:n.651+39_651+40delinsAG
XM_024446338.1:c.1056+39_1056+40delinsAG	XP_024302106.1:n.1056+39_1056+40delinsAG
NM_006623.4:c.945+39_945+40delinsAG MANE Select	NP_006614.2:n.945+39_945+40delinsAG