Canonical Allele Identifier: CA394695833

Gene: PMM2

Linked Data

• MyVariant Identifiers: chr16:g.8898642A>C (hg19) ; chr16:g.8804785A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8804785A>C , CM000678.2:g.8804785A>C	GRCh38
NC_000016.9:g.8898642A>C , CM000678.1:g.8898642A>C	GRCh37
NC_000016.8:g.8806143A>C	NCBI36
NG_009209.1:g.11973A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682008.1:c.197A>C	ENSP00000507849.1:p.Tyr66Ser
ENST00000682393.1:c.178+2875A>C	ENSP00000506774.1:n.178+2875A>C
ENST00000683094.1:c.179-1531A>C	ENSP00000508230.1:n.179-1531A>C
ENST00000683274.1:c.197A>C	ENSP00000507262.1:p.Tyr66Ser
ENST00000683435.1:c.*193A>C	ENSP00000508092.1:n.*193A>C
ENST00000268261.9:c.197A>C MANE Select	ENSP00000268261.4:p.Tyr66Ser
ENST00000268261.8:c.197A>C	ENSP00000268261.4:p.Tyr66Ser
ENST00000562318.5:c.179-1531A>C	ENSP00000454395.1:n.179-1531A>C
ENST00000562448.1:n.220-1531A>C
ENST00000564030.5:n.259A>C
ENST00000564069.1:c.168A>C
ENST00000565221.5:c.178+2875A>C	ENSP00000457932.1:n.178+2875A>C
ENST00000565896.5:c.*145+2396A>C	ENSP00000456024.1:n.*145+2396A>C
ENST00000566540.5:c.179-1531A>C	ENSP00000454284.1:n.179-1531A>C
ENST00000566604.5:c.197A>C	ENSP00000456774.1:p.Tyr66Ser
ENST00000566983.5:c.116A>C	ENSP00000457956.1:p.Tyr39Ser
ENST00000568602.5:c.*50A>C	ENSP00000455066.1:n.*50A>C
ENST00000569958.5:c.178+2875A>C	ENSP00000456302.1:n.178+2875A>C
ENST00000570076.5:c.178+2875A>C	ENSP00000456961.1:n.178+2875A>C
ENST00000570134.5:c.179-1531A>C	ENSP00000456275.1:n.179-1531A>C
NM_000303.2:c.197A>C	NP_000294.1:p.Tyr66Ser
XM_005255372.3:c.197A>C	XP_005255429.1:p.Tyr66Ser
XM_005255373.3:c.7-1531A>C	XP_005255430.1:n.7-1531A>C
XM_005255374.3:c.7-1531A>C	XP_005255431.1:n.7-1531A>C
XM_011522538.1:c.197A>C	XP_011520840.1:p.Tyr66Ser
XM_011522539.1:c.-29+2875A>C	XP_011520841.1:n.-29+2875A>C
XM_005255374.4:c.7-1531A>C	XP_005255431.1:n.7-1531A>C
NM_000303.3:c.197A>C MANE Select	NP_000294.1:p.Tyr66Ser