Canonical Allele Identifier: CA2206128225
Gene: PMM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.8797827C= , CM000678.2:g.8797827C= GRCh38
NC_000016.9:g.8891684C= , CM000678.1:g.8891684C= GRCh37
NC_000016.8:g.8799185C= NCBI36
NG_009209.1:g.5015C=
NG_033146.1:g.4822G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682008.1:c.-56C= ENSP00000507849.1:n.-56C=
ENST00000683435.1:c.-56C= ENSP00000508092.1:n.-56C=
ENST00000268261.8:c.-56C= ENSP00000268261.4:n.-56C=
ENST00000564030.5:n.7C=
ENST00000566983.5:c.-15-3972C= ENSP00000457956.1:n.-15-3972C=
NM_000303.2:c.-56C= NP_000294.1:n.-56C=
XM_005255372.3:c.-56C= XP_005255429.1:n.-56C=
XM_005255373.3:c.-228C= XP_005255430.1:n.-228C=
XM_005255374.3:c.-228C= XP_005255431.1:n.-228C=
XM_011522538.1:c.-56C= XP_011520840.1:n.-56C=
XM_005255374.4:c.-228C= XP_005255431.1:n.-228C=