Canonical Allele Identifier: CA2206132468

Gene: PMM2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8805053_8805056delinsTTTC , CM000678.2:g.8805053_8805056delinsTTTC	GRCh38
NC_000016.9:g.8898910_8898913delinsTTTC , CM000678.1:g.8898910_8898913delinsTTTC	GRCh37
NC_000016.8:g.8806411_8806414delinsTTTC	NCBI36
NG_009209.1:g.12241_12244delinsTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682008.1:c.255+210_255+213delinsTTTC	ENSP00000507849.1:n.255+210_255+213delinsTTTC
ENST00000682393.1:c.178+3143_178+3146delinsTTTC	ENSP00000506774.1:n.178+3143_178+3146delinsTTTC
ENST00000683094.1:c.179-1263_179-1260delinsTTTC	ENSP00000508230.1:n.179-1263_179-1260delinsTTTC
ENST00000683274.1:c.255+210_255+213delinsTTTC	ENSP00000507262.1:n.255+210_255+213delinsTTTC
ENST00000683435.1:c.*251+210_*251+213delinsTTTC	ENSP00000508092.1:n.*251+210_*251+213delinsTTTC
ENST00000268261.9:c.255+210_255+213delinsTTTC MANE Select	ENSP00000268261.4:n.255+210_255+213delinsTTTC
ENST00000268261.8:c.255+210_255+213delinsTTTC	ENSP00000268261.4:n.255+210_255+213delinsTTTC
ENST00000562318.5:c.179-1263_179-1260delinsTTTC	ENSP00000454395.1:n.179-1263_179-1260delinsTTTC
ENST00000562448.1:n.220-1263_220-1260delinsTTTC
ENST00000564030.5:n.317+210_317+213delinsTTTC
ENST00000564069.1:c.226+210_226+213delinsTTTC
ENST00000565221.5:c.178+3143_178+3146delinsTTTC	ENSP00000457932.1:n.178+3143_178+3146delinsTTTC
ENST00000565896.5:c.*145+2664_*145+2667delinsTTTC	ENSP00000456024.1:n.*145+2664_*145+2667delinsTTTC
ENST00000566540.5:c.179-1263_179-1260delinsTTTC	ENSP00000454284.1:n.179-1263_179-1260delinsTTTC
ENST00000566604.5:c.255+210_255+213delinsTTTC	ENSP00000456774.1:n.255+210_255+213delinsTTTC
ENST00000566983.5:c.174+210_174+213delinsTTTC	ENSP00000457956.1:n.174+210_174+213delinsTTTC
ENST00000568602.5:c.*108+210_*108+213delinsTTTC	ENSP00000455066.1:n.*108+210_*108+213delinsTTTC
ENST00000569958.5:c.178+3143_178+3146delinsTTTC	ENSP00000456302.1:n.178+3143_178+3146delinsTTTC
ENST00000570076.5:c.178+3143_178+3146delinsTTTC	ENSP00000456961.1:n.178+3143_178+3146delinsTTTC
ENST00000570134.5:c.179-1263_179-1260delinsTTTC	ENSP00000456275.1:n.179-1263_179-1260delinsTTTC
NM_000303.2:c.255+210_255+213delinsTTTC	NP_000294.1:n.255+210_255+213delinsTTTC
XM_005255372.3:c.255+210_255+213delinsTTTC	XP_005255429.1:n.255+210_255+213delinsTTTC
XM_005255373.3:c.7-1263_7-1260delinsTTTC	XP_005255430.1:n.7-1263_7-1260delinsTTTC
XM_005255374.3:c.7-1263_7-1260delinsTTTC	XP_005255431.1:n.7-1263_7-1260delinsTTTC
XM_011522538.1:c.255+210_255+213delinsTTTC	XP_011520840.1:n.255+210_255+213delinsTTTC
XM_011522539.1:c.-29+3143_-29+3146delinsTTTC	XP_011520841.1:n.-29+3143_-29+3146delinsTTTC
XM_005255374.4:c.7-1263_7-1260delinsTTTC	XP_005255431.1:n.7-1263_7-1260delinsTTTC
NM_000303.3:c.255+210_255+213delinsTTTC MANE Select	NP_000294.1:n.255+210_255+213delinsTTTC