Canonical Allele Identifier: CA341851083

Gene: PHGDH

Linked Data

• MyVariant Identifiers: chr1:g.120279741C>A (hg19) ; chr1:g.119737118C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119737118C>A , CM000663.2:g.119737118C>A	GRCh38
NC_000001.10:g.120279741C>A , CM000663.1:g.120279741C>A	GRCh37
NC_000001.9:g.120081264C>A	NCBI36
NG_009188.1:g.30323C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.797C>A	ENSP00000358417.5:p.Pro266Gln
ENST00000469443.2:n.617C>A
ENST00000641023.2:c.797C>A MANE Select	ENSP00000493175.1:p.Pro266Gln
ENST00000641074.1:c.797C>A	ENSP00000493446.1:p.Pro266Gln
ENST00000641115.1:c.797C>A	ENSP00000493264.1:p.Pro266Gln
ENST00000641213.1:c.*450C>A	ENSP00000493079.1:n.*450C>A
ENST00000641314.1:n.782C>A
ENST00000641375.1:c.*633C>A	ENSP00000493089.1:n.*633C>A
ENST00000641597.1:c.797C>A	ENSP00000493382.1:p.Pro266Gln
ENST00000641756.1:c.*541C>A	ENSP00000493147.1:n.*541C>A
ENST00000641811.1:c.553C>A
ENST00000641891.1:c.*623C>A	ENSP00000493288.1:n.*623C>A
ENST00000641927.1:n.737C>A
ENST00000641947.1:c.797C>A	ENSP00000492994.1:p.Pro266Gln
ENST00000642021.1:n.919C>A
ENST00000369407.3:c.695C>A	ENSP00000358415.3:p.Pro232Gln
ENST00000369409.8:c.797C>A	ENSP00000358417.4:p.Pro266Gln
NM_006623.3:c.797C>A	NP_006614.2:p.Pro266Gln
XM_011541226.1:c.1019C>A	XP_011539528.1:p.Pro340Gln
XM_011541227.1:c.941C>A	XP_011539529.1:p.Pro314Gln
XM_011541228.1:c.908C>A	XP_011539530.1:p.Pro303Gln
XM_011541229.1:c.734C>A	XP_011539531.1:p.Pro245Gln
XM_011541230.1:c.512C>A	XP_011539532.1:p.Pro171Gln
XM_011541231.1:c.503C>A	XP_011539533.1:p.Pro168Gln
XM_011541226.2:c.1019C>A	XP_011539528.1:p.Pro340Gln
XM_011541227.2:c.941C>A	XP_011539529.1:p.Pro314Gln
XM_011541228.2:c.908C>A	XP_011539530.1:p.Pro303Gln
XM_011541231.2:c.503C>A	XP_011539533.1:p.Pro168Gln
XM_024446338.1:c.908C>A	XP_024302106.1:p.Pro303Gln
NM_006623.4:c.797C>A MANE Select	NP_006614.2:p.Pro266Gln