Canonical Allele Identifier: CA277493569

Gene: PMM2

Linked Data

• dbSNP Id: rs574266342
• gnomAD v2: 16-8941430-C-G
• gnomAD v3: 16-8847573-C-G
• gnomAD v4: 16-8847573-C-G
• MyVariant Identifiers: chr16:g.8941430C>G (hg19) ; chr16:g.8847573C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8847573C>G , CM000678.2:g.8847573C>G	GRCh38
NC_000016.9:g.8941430C>G , CM000678.1:g.8941430C>G	GRCh37
NC_000016.8:g.8848931C>G	NCBI36
NG_009209.1:g.54761C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000567697.2:n.3808-151C>G
ENST00000682393.1:c.*258-1796C>G	ENSP00000506774.1:n.*258-1796C>G
ENST00000683094.1:c.*262-1796C>G	ENSP00000508230.1:n.*262-1796C>G
ENST00000683274.1:c.*180-1796C>G	ENSP00000507262.1:n.*180-1796C>G
ENST00000683435.1:c.*536-151C>G	ENSP00000508092.1:n.*536-151C>G
ENST00000268261.9:c.640-151C>G MANE Select	ENSP00000268261.4:n.640-151C>G
ENST00000268261.8:c.640-151C>G	ENSP00000268261.4:n.640-151C>G
ENST00000562025.1:n.174-151C>G
ENST00000562318.5:c.*362-151C>G	ENSP00000454395.1:n.*362-151C>G
ENST00000565221.5:c.*258-151C>G	ENSP00000457932.1:n.*258-151C>G
ENST00000566540.5:c.*262-151C>G	ENSP00000454284.1:n.*262-151C>G
ENST00000566604.5:c.*180-151C>G	ENSP00000456774.1:n.*180-151C>G
ENST00000566983.5:c.559-151C>G	ENSP00000457956.1:n.559-151C>G
ENST00000567697.1:n.3808-151C>G
ENST00000569958.5:c.367-151C>G	ENSP00000456302.1:n.367-151C>G
ENST00000570076.5:c.*98-151C>G	ENSP00000456961.1:n.*98-151C>G
NM_000303.2:c.640-151C>G	NP_000294.1:n.640-151C>G
XM_005255374.3:c.391-151C>G	XP_005255431.1:n.391-151C>G
XM_011522538.1:c.640-7461C>G	XP_011520840.1:n.640-7461C>G
XM_005255374.4:c.391-151C>G	XP_005255431.1:n.391-151C>G
NM_000303.3:c.640-151C>G MANE Select	NP_000294.1:n.640-151C>G