Canonical Allele Identifier: CA1978914000
Gene: PYGM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64750595C= , CM000673.2:g.64750595C= GRCh38
NC_000011.9:g.64518067C= , CM000673.1:g.64518067C= GRCh37
NC_000011.8:g.64274643C= NCBI36
NG_013018.1:g.15121G=

Transcript Alleles

HGVS Amino-acid change
ENST00000164139.4:c.1970-12G= MANE Select ENSP00000164139.3:n.1970-12G=
ENST00000164139.3:c.1970-12G= ENSP00000164139.3:n.1970-12G=
ENST00000377432.7:c.1706-12G= ENSP00000366650.3:n.1706-12G=
NM_001164716.1:c.1706-12G= NP_001158188.1:n.1706-12G=
NM_005609.2:c.1970-12G= NP_005600.1:n.1970-12G=
NM_005609.3:c.1970-12G= NP_005600.1:n.1970-12G=
NM_005609.4:c.1970-12G= MANE Select NP_005600.1:n.1970-12G=