Canonical Allele Identifier: CA2575906605

Gene: PMM2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8847645T>C , CM000678.2:g.8847645T>C	GRCh38
NC_000016.9:g.8941502T>C , CM000678.1:g.8941502T>C	GRCh37
NC_000016.8:g.8849003T>C	NCBI36
NG_009209.1:g.54833T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567697.2:n.3808-79T>C
ENST00000682393.1:c.*258-1724T>C	ENSP00000506774.1:n.*258-1724T>C
ENST00000683094.1:c.*262-1724T>C	ENSP00000508230.1:n.*262-1724T>C
ENST00000683274.1:c.*180-1724T>C	ENSP00000507262.1:n.*180-1724T>C
ENST00000683435.1:c.*536-79T>C	ENSP00000508092.1:n.*536-79T>C
ENST00000268261.9:c.640-79T>C MANE Select	ENSP00000268261.4:n.640-79T>C
ENST00000268261.8:c.640-79T>C	ENSP00000268261.4:n.640-79T>C
ENST00000562025.1:n.174-79T>C
ENST00000562318.5:c.*362-79T>C	ENSP00000454395.1:n.*362-79T>C
ENST00000565221.5:c.*258-79T>C	ENSP00000457932.1:n.*258-79T>C
ENST00000566540.5:c.*262-79T>C	ENSP00000454284.1:n.*262-79T>C
ENST00000566604.5:c.*180-79T>C	ENSP00000456774.1:n.*180-79T>C
ENST00000566983.5:c.559-79T>C	ENSP00000457956.1:n.559-79T>C
ENST00000567697.1:n.3808-79T>C
ENST00000569958.5:c.367-79T>C	ENSP00000456302.1:n.367-79T>C
ENST00000570076.5:c.*98-79T>C	ENSP00000456961.1:n.*98-79T>C
NM_000303.2:c.640-79T>C	NP_000294.1:n.640-79T>C
XM_005255374.3:c.391-79T>C	XP_005255431.1:n.391-79T>C
XM_011522538.1:c.640-7389T>C	XP_011520840.1:n.640-7389T>C
XM_005255374.4:c.391-79T>C	XP_005255431.1:n.391-79T>C
NM_000303.3:c.640-79T>C MANE Select	NP_000294.1:n.640-79T>C