Canonical Allele Identifier: CA394694746

Gene: PMM2

Linked Data

• gnomAD v4: 16-8797884-T-C
• MyVariant Identifiers: chr16:g.8891741T>C (hg19) ; chr16:g.8797884T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8797884T>C , CM000678.2:g.8797884T>C	GRCh38
NC_000016.9:g.8891741T>C , CM000678.1:g.8891741T>C	GRCh37
NC_000016.8:g.8799242T>C	NCBI36
NG_009209.1:g.5072T>C
NG_033146.1:g.4765A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682008.1:c.2T>C	ENSP00000507849.1:p.Met1Thr
ENST00000682393.1:c.2T>C	ENSP00000506774.1:p.Met1Thr
ENST00000683094.1:c.2T>C	ENSP00000508230.1:p.Met1Thr
ENST00000683274.1:c.2T>C	ENSP00000507262.1:p.Met1Thr
ENST00000683435.1:c.2T>C	ENSP00000508092.1:p.Met1Thr
ENST00000268261.9:c.2T>C MANE Select	ENSP00000268261.4:p.Met1Thr
ENST00000268261.8:c.2T>C	ENSP00000268261.4:p.Met1Thr
ENST00000562318.5:c.2T>C	ENSP00000454395.1:p.Met1Thr
ENST00000562448.1:n.43T>C
ENST00000564030.5:n.64T>C
ENST00000565221.5:c.2T>C	ENSP00000457932.1:p.Met1Thr
ENST00000565896.5:c.2T>C	ENSP00000456024.1:p.Met1Thr
ENST00000566196.5:n.46T>C
ENST00000566540.5:c.2T>C	ENSP00000454284.1:p.Met1Thr
ENST00000566604.5:c.2T>C	ENSP00000456774.1:p.Met1Thr
ENST00000566983.5:c.-15-3915T>C	ENSP00000457956.1:n.-15-3915T>C
ENST00000568602.5:c.2T>C	ENSP00000455066.1:p.Met1Thr
ENST00000569958.5:c.2T>C	ENSP00000456302.1:p.Met1Thr
ENST00000570076.5:c.2T>C	ENSP00000456961.1:p.Met1Thr
ENST00000570134.5:c.2T>C	ENSP00000456275.1:p.Met1Thr
NM_000303.2:c.2T>C	NP_000294.1:p.Met1Thr
XM_005255372.3:c.2T>C	XP_005255429.1:p.Met1Thr
XM_005255373.3:c.-171T>C	XP_005255430.1:n.-171T>C
XM_005255374.3:c.-171T>C	XP_005255431.1:n.-171T>C
XM_011522538.1:c.2T>C	XP_011520840.1:p.Met1Thr
XM_005255374.4:c.-171T>C	XP_005255431.1:n.-171T>C
NM_000303.3:c.2T>C MANE Select	NP_000294.1:p.Met1Thr