Canonical Allele Identifier: CA620730270

Gene: PMM2

Linked Data

• dbSNP Id: rs1185565868
• gnomAD v2: 16-8904876-C-CCA
• gnomAD v3: 16-8811019-C-CCA
• gnomAD v4: 16-8811019-C-CCA
• MyVariant Identifiers: chr16:g.8904876_8904877insCA (hg19) ; chr16:g.8811019_8811020insCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8811019_8811020insCA , CM000678.2:g.8811019_8811020insCA	GRCh38
NC_000016.9:g.8904876_8904877insCA , CM000678.1:g.8904876_8904877insCA	GRCh37
NC_000016.8:g.8812377_8812378insCA	NCBI36
NG_009209.1:g.18207_18208insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567697.2:n.3456_3457insCA
ENST00000682008.1:c.348-60_348-59insCA	ENSP00000507849.1:n.348-60_348-59insCA
ENST00000682393.1:c.179-60_179-59insCA	ENSP00000506774.1:n.179-60_179-59insCA
ENST00000683094.1:c.*70-619_*70-618insCA	ENSP00000508230.1:n.*70-619_*70-618insCA
ENST00000683274.1:c.348-619_348-618insCA	ENSP00000507262.1:n.348-619_348-618insCA
ENST00000683435.1:c.*344-619_*344-618insCA	ENSP00000508092.1:n.*344-619_*344-618insCA
ENST00000268261.9:c.348-60_348-59insCA MANE Select	ENSP00000268261.4:n.348-60_348-59insCA
ENST00000268261.8:c.348-60_348-59insCA	ENSP00000268261.4:n.348-60_348-59insCA
ENST00000562318.5:c.*70-60_*70-59insCA	ENSP00000454395.1:n.*70-60_*70-59insCA
ENST00000564069.1:c.319-60_319-59insCA
ENST00000565221.5:c.179-60_179-59insCA	ENSP00000457932.1:n.179-60_179-59insCA
ENST00000565896.5:c.*146-60_*146-59insCA	ENSP00000456024.1:n.*146-60_*146-59insCA
ENST00000566540.5:c.*70-619_*70-618insCA	ENSP00000454284.1:n.*70-619_*70-618insCA
ENST00000566604.5:c.348-619_348-618insCA	ENSP00000456774.1:n.348-619_348-618insCA
ENST00000566983.5:c.267-60_267-59insCA	ENSP00000457956.1:n.267-60_267-59insCA
ENST00000567697.1:n.3456_3457insCA
ENST00000568602.5:c.*201-60_*201-59insCA	ENSP00000455066.1:n.*201-60_*201-59insCA
ENST00000569958.5:c.179-623_179-622insCA	ENSP00000456302.1:n.179-623_179-622insCA
ENST00000570076.5:c.179-619_179-618insCA	ENSP00000456961.1:n.179-619_179-618insCA
ENST00000570134.5:c.*70-619_*70-618insCA	ENSP00000456275.1:n.*70-619_*70-618insCA
NM_000303.2:c.348-60_348-59insCA	NP_000294.1:n.348-60_348-59insCA
XM_005255372.3:c.348-60_348-59insCA	XP_005255429.1:n.348-60_348-59insCA
XM_005255373.3:c.99-60_99-59insCA	XP_005255430.1:n.99-60_99-59insCA
XM_005255374.3:c.99-60_99-59insCA	XP_005255431.1:n.99-60_99-59insCA
XM_011522538.1:c.348-60_348-59insCA	XP_011520840.1:n.348-60_348-59insCA
XM_011522539.1:c.-28-60_-28-59insCA	XP_011520841.1:n.-28-60_-28-59insCA
XM_005255374.4:c.99-60_99-59insCA	XP_005255431.1:n.99-60_99-59insCA
NM_000303.3:c.348-60_348-59insCA MANE Select	NP_000294.1:n.348-60_348-59insCA