Canonical Allele Identifier: CA394696677

Gene: PMM2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8811163C>A , CM000678.2:g.8811163C>A	GRCh38
NC_000016.9:g.8905020C>A , CM000678.1:g.8905020C>A	GRCh37
NC_000016.8:g.8812521C>A	NCBI36
NG_009209.1:g.18351C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567697.2:n.3600C>A
ENST00000682008.1:c.432C>A	ENSP00000507849.1:p.Phe144Leu
ENST00000682393.1:c.*50C>A	ENSP00000506774.1:n.*50C>A
ENST00000683094.1:c.*70-475C>A	ENSP00000508230.1:n.*70-475C>A
ENST00000683274.1:c.348-475C>A	ENSP00000507262.1:n.348-475C>A
ENST00000683435.1:c.*344-475C>A	ENSP00000508092.1:n.*344-475C>A
ENST00000268261.9:c.432C>A MANE Select	ENSP00000268261.4:p.Phe144Leu
ENST00000268261.8:c.432C>A	ENSP00000268261.4:p.Phe144Leu
ENST00000562318.5:c.*154C>A	ENSP00000454395.1:n.*154C>A
ENST00000564069.1:c.403C>A
ENST00000565221.5:c.*50C>A	ENSP00000457932.1:n.*50C>A
ENST00000565896.5:c.*230C>A	ENSP00000456024.1:n.*230C>A
ENST00000566540.5:c.*70-475C>A	ENSP00000454284.1:n.*70-475C>A
ENST00000566604.5:c.348-475C>A	ENSP00000456774.1:n.348-475C>A
ENST00000566983.5:c.351C>A	ENSP00000457956.1:p.Phe117Leu
ENST00000567697.1:n.3600C>A
ENST00000569958.5:c.179-479C>A	ENSP00000456302.1:n.179-479C>A
ENST00000570076.5:c.179-475C>A	ENSP00000456961.1:n.179-475C>A
ENST00000570134.5:c.*70-475C>A	ENSP00000456275.1:n.*70-475C>A
NM_000303.2:c.432C>A	NP_000294.1:p.Phe144Leu
XM_005255372.3:c.432C>A	XP_005255429.1:p.Phe144Leu
XM_005255373.3:c.183C>A	XP_005255430.1:p.Phe61Leu
XM_005255374.3:c.183C>A	XP_005255431.1:p.Phe61Leu
XM_011522538.1:c.432C>A	XP_011520840.1:p.Phe144Leu
XM_011522539.1:c.57C>A	XP_011520841.1:p.Phe19Leu
XM_005255374.4:c.183C>A	XP_005255431.1:p.Phe61Leu
NM_000303.3:c.432C>A MANE Select	NP_000294.1:p.Phe144Leu