Canonical Allele Identifier: CA493489712

Gene: PMM2

Linked Data

• MyVariant Identifiers: chr16:g.8941800G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8847943G>C , CM000678.2:g.8847943G>C	GRCh38
NC_000016.9:g.8941800G>C , CM000678.1:g.8941800G>C	GRCh37
NC_000016.8:g.8849301G>C	NCBI36
NG_009209.1:g.55131G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567697.2:n.4027G>C
ENST00000682393.1:c.*258-1426G>C	ENSP00000506774.1:n.*258-1426G>C
ENST00000683094.1:c.*262-1426G>C	ENSP00000508230.1:n.*262-1426G>C
ENST00000683274.1:c.*180-1426G>C	ENSP00000507262.1:n.*180-1426G>C
ENST00000683435.1:c.*755G>C	ENSP00000508092.1:n.*755G>C
ENST00000268261.9:c.*118G>C MANE Select	ENSP00000268261.4:n.*118G>C
ENST00000268261.8:c.*118G>C	ENSP00000268261.4:n.*118G>C
ENST00000562025.1:n.393G>C
ENST00000562318.5:c.*581G>C	ENSP00000454395.1:n.*581G>C
ENST00000565221.5:c.*477G>C	ENSP00000457932.1:n.*477G>C
ENST00000566540.5:c.*481G>C	ENSP00000454284.1:n.*481G>C
ENST00000566604.5:c.*399G>C	ENSP00000456774.1:n.*399G>C
ENST00000567697.1:n.4027G>C
ENST00000569958.5:c.*118G>C	ENSP00000456302.1:n.*118G>C
ENST00000570076.5:c.*317G>C	ENSP00000456961.1:n.*317G>C
NM_000303.2:c.*118G>C	NP_000294.1:n.*118G>C
XM_005255374.3:c.*118G>C	XP_005255431.1:n.*118G>C
XM_011522538.1:c.640-7091G>C	XP_011520840.1:n.640-7091G>C
XM_005255374.4:c.*118G>C	XP_005255431.1:n.*118G>C
NM_000303.3:c.*118G>C MANE Select	NP_000294.1:n.*118G>C