Canonical Allele Identifier: CA341854213

Gene: PHGDH

Linked Data

• MyVariant Identifiers: chr1:g.120286538C>A (hg19) ; chr1:g.119743915C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119743915C>A , CM000663.2:g.119743915C>A	GRCh38
NC_000001.10:g.120286538C>A , CM000663.1:g.120286538C>A	GRCh37
NC_000001.9:g.120088061C>A	NCBI36
NG_009188.1:g.37120C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369409.9:c.1496C>A	ENSP00000358417.5:p.Ala499Asp
ENST00000641023.2:c.1477C>A MANE Select	ENSP00000493175.1:p.Leu493Met
ENST00000641074.1:c.*56C>A	ENSP00000493446.1:n.*56C>A
ENST00000641115.1:c.1213C>A	ENSP00000493264.1:p.Leu405Met
ENST00000641213.1:c.*1130C>A	ENSP00000493079.1:n.*1130C>A
ENST00000641314.1:n.1462C>A
ENST00000641375.1:c.*1313C>A	ENSP00000493089.1:n.*1313C>A
ENST00000641597.1:c.1477C>A	ENSP00000493382.1:p.Leu493Met
ENST00000641756.1:c.*1221C>A	ENSP00000493147.1:n.*1221C>A
ENST00000641811.1:c.731C>A
ENST00000641891.1:c.*1303C>A	ENSP00000493288.1:n.*1303C>A
ENST00000641927.1:n.1417C>A
ENST00000641947.1:c.1456C>A	ENSP00000492994.1:p.Leu486Met
ENST00000642021.1:n.2508C>A
ENST00000369407.3:c.1375C>A	ENSP00000358415.3:p.Leu459Met
ENST00000369409.8:c.1477C>A	ENSP00000358417.4:p.Leu493Met
ENST00000482968.1:n.1456C>A
NM_006623.3:c.1477C>A	NP_006614.2:p.Leu493Met
XM_011541226.1:c.1699C>A	XP_011539528.1:p.Leu567Met
XM_011541227.1:c.1621C>A	XP_011539529.1:p.Leu541Met
XM_011541228.1:c.1588C>A	XP_011539530.1:p.Leu530Met
XM_011541229.1:c.1414C>A	XP_011539531.1:p.Leu472Met
XM_011541230.1:c.1192C>A	XP_011539532.1:p.Leu398Met
XM_011541231.1:c.1183C>A	XP_011539533.1:p.Leu395Met
XM_011541226.2:c.1699C>A	XP_011539528.1:p.Leu567Met
XM_011541227.2:c.1621C>A	XP_011539529.1:p.Leu541Met
XM_011541228.2:c.1588C>A	XP_011539530.1:p.Leu530Met
XM_011541231.2:c.1183C>A	XP_011539533.1:p.Leu395Met
XM_024446338.1:c.1588C>A	XP_024302106.1:p.Leu530Met
NM_006623.4:c.1477C>A MANE Select	NP_006614.2:p.Leu493Met