Canonical Allele Identifier: CA2631646119

Gene: PMM2

Linked Data

• gnomAD v4: 16-8847649-G-GGACT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8847650_8847653dup , CM000678.2:g.8847650_8847653dup	GRCh38
NC_000016.9:g.8941507_8941510dup , CM000678.1:g.8941507_8941510dup	GRCh37
NC_000016.8:g.8849008_8849011dup	NCBI36
NG_009209.1:g.54838_54841dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567697.2:n.3808-74_3808-71dup
ENST00000682393.1:c.*258-1719_*258-1716dup	ENSP00000506774.1:n.*258-1719_*258-1716dup
ENST00000683094.1:c.*262-1719_*262-1716dup	ENSP00000508230.1:n.*262-1719_*262-1716dup
ENST00000683274.1:c.*180-1719_*180-1716dup	ENSP00000507262.1:n.*180-1719_*180-1716dup
ENST00000683435.1:c.*536-74_*536-71dup	ENSP00000508092.1:n.*536-74_*536-71dup
ENST00000268261.9:c.640-74_640-71dup MANE Select	ENSP00000268261.4:n.640-74_640-71dup
ENST00000268261.8:c.640-74_640-71dup	ENSP00000268261.4:n.640-74_640-71dup
ENST00000562025.1:n.174-74_174-71dup
ENST00000562318.5:c.*362-74_*362-71dup	ENSP00000454395.1:n.*362-74_*362-71dup
ENST00000565221.5:c.*258-74_*258-71dup	ENSP00000457932.1:n.*258-74_*258-71dup
ENST00000566540.5:c.*262-74_*262-71dup	ENSP00000454284.1:n.*262-74_*262-71dup
ENST00000566604.5:c.*180-74_*180-71dup	ENSP00000456774.1:n.*180-74_*180-71dup
ENST00000566983.5:c.559-74_559-71dup	ENSP00000457956.1:n.559-74_559-71dup
ENST00000567697.1:n.3808-74_3808-71dup
ENST00000569958.5:c.367-74_367-71dup	ENSP00000456302.1:n.367-74_367-71dup
ENST00000570076.5:c.*98-74_*98-71dup	ENSP00000456961.1:n.*98-74_*98-71dup
NM_000303.2:c.640-74_640-71dup	NP_000294.1:n.640-74_640-71dup
XM_005255374.3:c.391-74_391-71dup	XP_005255431.1:n.391-74_391-71dup
XM_011522538.1:c.640-7384_640-7381dup	XP_011520840.1:n.640-7384_640-7381dup
XM_005255374.4:c.391-74_391-71dup	XP_005255431.1:n.391-74_391-71dup
NM_000303.3:c.640-74_640-71dup MANE Select	NP_000294.1:n.640-74_640-71dup