Canonical Allele Identifier: CA1978913173
Gene: PYGM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64750422_64750425delinsTGAA , CM000673.2:g.64750422_64750425delinsTGAA GRCh38
NC_000011.9:g.64517894_64517897delinsTGAA , CM000673.1:g.64517894_64517897delinsTGAA GRCh37
NC_000011.8:g.64274470_64274473delinsTGAA NCBI36
NG_007574.1:g.32_35delinsTTCA , LRG_100:g.32_35delinsTTCA
NG_013018.1:g.15291_15294delinsTTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.2128_2131delinsTTCA MANE Select ENSP00000164139.3:p.Phe710=
ENST00000164139.3:c.2128_2131delinsTTCA ENSP00000164139.3:p.Phe710=
ENST00000377432.7:c.1864_1867delinsTTCA ENSP00000366650.3:p.Phe622=
NM_001164716.1:c.1864_1867delinsTTCA NP_001158188.1:p.Phe622=
NM_005609.2:c.2128_2131delinsTTCA NP_005600.1:p.Phe710=
NM_005609.3:c.2128_2131delinsTTCA NP_005600.1:p.Phe710=
NM_005609.4:c.2128_2131delinsTTCA MANE Select NP_005600.1:p.Phe710=