Canonical Allele Identifier: CA2614191269
Gene: PYGM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64758737dup , CM000673.2:g.64758737dup GRCh38
NC_000011.9:g.64526209dup , CM000673.1:g.64526209dup GRCh37
NC_000011.8:g.64282785dup NCBI36
NG_013018.1:g.6982dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.244-30dup MANE Select ENSP00000164139.3:n.244-30dup
ENST00000164139.3:c.244-30dup ENSP00000164139.3:n.244-30dup
ENST00000377432.7:c.244-468dup ENSP00000366650.3:n.244-468dup
NM_001164716.1:c.244-468dup NP_001158188.1:n.244-468dup
NM_005609.2:c.244-30dup NP_005600.1:n.244-30dup
NM_005609.3:c.244-30dup NP_005600.1:n.244-30dup
NM_005609.4:c.244-30dup MANE Select NP_005600.1:n.244-30dup