Canonical Allele Identifier: CA2631646197

Gene: PMM2

Linked Data

• gnomAD v4: 16-8848032-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8848032G>T , CM000678.2:g.8848032G>T	GRCh38
NC_000016.9:g.8941889G>T , CM000678.1:g.8941889G>T	GRCh37
NC_000016.8:g.8849390G>T	NCBI36
NG_009209.1:g.55220G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567697.2:n.4116G>T
ENST00000682393.1:c.*258-1337G>T	ENSP00000506774.1:n.*258-1337G>T
ENST00000683094.1:c.*262-1337G>T	ENSP00000508230.1:n.*262-1337G>T
ENST00000683274.1:c.*180-1337G>T	ENSP00000507262.1:n.*180-1337G>T
ENST00000268261.9:c.*207G>T MANE Select	ENSP00000268261.4:n.*207G>T
ENST00000268261.8:c.*207G>T	ENSP00000268261.4:n.*207G>T
ENST00000562025.1:n.482G>T
ENST00000562318.5:c.*670G>T	ENSP00000454395.1:n.*670G>T
ENST00000566540.5:c.*570G>T	ENSP00000454284.1:n.*570G>T
ENST00000566604.5:c.*488G>T	ENSP00000456774.1:n.*488G>T
ENST00000567697.1:n.4116G>T
ENST00000569958.5:c.*207G>T	ENSP00000456302.1:n.*207G>T
ENST00000570076.5:c.*406G>T	ENSP00000456961.1:n.*406G>T
NM_000303.2:c.*207G>T	NP_000294.1:n.*207G>T
XM_005255374.3:c.*207G>T	XP_005255431.1:n.*207G>T
XM_011522538.1:c.640-7002G>T	XP_011520840.1:n.640-7002G>T
XM_005255374.4:c.*207G>T	XP_005255431.1:n.*207G>T
NM_000303.3:c.*207G>T MANE Select	NP_000294.1:n.*207G>T