Canonical Allele Identifier: CA2206157964

Gene: PMM2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8847586T= , CM000678.2:g.8847586T=	GRCh38
NC_000016.9:g.8941443T= , CM000678.1:g.8941443T=	GRCh37
NC_000016.8:g.8848944T=	NCBI36
NG_009209.1:g.54774T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567697.2:n.3808-138T=
ENST00000682393.1:c.*258-1783T=	ENSP00000506774.1:n.*258-1783T=
ENST00000683094.1:c.*262-1783T=	ENSP00000508230.1:n.*262-1783T=
ENST00000683274.1:c.*180-1783T=	ENSP00000507262.1:n.*180-1783T=
ENST00000683435.1:c.*536-138T=	ENSP00000508092.1:n.*536-138T=
ENST00000268261.9:c.640-138T= MANE Select	ENSP00000268261.4:n.640-138T=
ENST00000268261.8:c.640-138T=	ENSP00000268261.4:n.640-138T=
ENST00000562025.1:n.174-138T=
ENST00000562318.5:c.*362-138T=	ENSP00000454395.1:n.*362-138T=
ENST00000565221.5:c.*258-138T=	ENSP00000457932.1:n.*258-138T=
ENST00000566540.5:c.*262-138T=	ENSP00000454284.1:n.*262-138T=
ENST00000566604.5:c.*180-138T=	ENSP00000456774.1:n.*180-138T=
ENST00000566983.5:c.559-138T=	ENSP00000457956.1:n.559-138T=
ENST00000567697.1:n.3808-138T=
ENST00000569958.5:c.367-138T=	ENSP00000456302.1:n.367-138T=
ENST00000570076.5:c.*98-138T=	ENSP00000456961.1:n.*98-138T=
NM_000303.2:c.640-138T=	NP_000294.1:n.640-138T=
XM_005255374.3:c.391-138T=	XP_005255431.1:n.391-138T=
XM_011522538.1:c.640-7448T=	XP_011520840.1:n.640-7448T=
XM_005255374.4:c.391-138T=	XP_005255431.1:n.391-138T=
NM_000303.3:c.640-138T= MANE Select	NP_000294.1:n.640-138T=