Canonical Allele Identifier: CA394696501

Gene: PMM2

Linked Data

• dbSNP Id: rs2060674564
• MyVariant Identifiers: chr16:g.8904941C>T (hg19) ; chr16:g.8811084C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8811084C>T , CM000678.2:g.8811084C>T	GRCh38
NC_000016.9:g.8904941C>T , CM000678.1:g.8904941C>T	GRCh37
NC_000016.8:g.8812442C>T	NCBI36
NG_009209.1:g.18272C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567697.2:n.3521C>T
ENST00000682008.1:c.353C>T	ENSP00000507849.1:p.Thr118Ile
ENST00000682393.1:c.184C>T	ENSP00000506774.1:p.Leu62Phe
ENST00000683094.1:c.*70-554C>T	ENSP00000508230.1:n.*70-554C>T
ENST00000683274.1:c.348-554C>T	ENSP00000507262.1:n.348-554C>T
ENST00000683435.1:c.*344-554C>T	ENSP00000508092.1:n.*344-554C>T
ENST00000268261.9:c.353C>T MANE Select	ENSP00000268261.4:p.Thr118Ile
ENST00000268261.8:c.353C>T	ENSP00000268261.4:p.Thr118Ile
ENST00000562318.5:c.*75C>T	ENSP00000454395.1:n.*75C>T
ENST00000564069.1:c.324C>T
ENST00000565221.5:c.184C>T	ENSP00000457932.1:p.Leu62Phe
ENST00000565896.5:c.*151C>T	ENSP00000456024.1:n.*151C>T
ENST00000566540.5:c.*70-554C>T	ENSP00000454284.1:n.*70-554C>T
ENST00000566604.5:c.348-554C>T	ENSP00000456774.1:n.348-554C>T
ENST00000566983.5:c.272C>T	ENSP00000457956.1:p.Thr91Ile
ENST00000567697.1:n.3521C>T
ENST00000568602.5:c.*206C>T	ENSP00000455066.1:n.*206C>T
ENST00000569958.5:c.179-558C>T	ENSP00000456302.1:n.179-558C>T
ENST00000570076.5:c.179-554C>T	ENSP00000456961.1:n.179-554C>T
ENST00000570134.5:c.*70-554C>T	ENSP00000456275.1:n.*70-554C>T
NM_000303.2:c.353C>T	NP_000294.1:p.Thr118Ile
XM_005255372.3:c.353C>T	XP_005255429.1:p.Thr118Ile
XM_005255373.3:c.104C>T	XP_005255430.1:p.Thr35Ile
XM_005255374.3:c.104C>T	XP_005255431.1:p.Thr35Ile
XM_011522538.1:c.353C>T	XP_011520840.1:p.Thr118Ile
XM_011522539.1:c.-23C>T	XP_011520841.1:n.-23C>T
XM_005255374.4:c.104C>T	XP_005255431.1:p.Thr35Ile
NM_000303.3:c.353C>T MANE Select	NP_000294.1:p.Thr118Ile