Canonical Allele Identifier: CA1978929912

Gene: PYGM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64759760C= , CM000673.2:g.64759760C=	GRCh38
NC_000011.9:g.64527232C= , CM000673.1:g.64527232C=	GRCh37
NC_000011.8:g.64283808C=	NCBI36
NG_013018.1:g.5956G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000164139.4:c.139G= MANE Select	ENSP00000164139.3:p.Ala47=
ENST00000164139.3:c.139G=	ENSP00000164139.3:p.Ala47=
ENST00000377432.7:c.139G=	ENSP00000366650.3:p.Ala47=
NM_001164716.1:c.139G=	NP_001158188.1:p.Ala47=
NM_005609.2:c.139G=	NP_005600.1:p.Ala47=
NM_005609.3:c.139G=	NP_005600.1:p.Ala47=
NM_005609.4:c.139G= MANE Select	NP_005600.1:p.Ala47=