Canonical Allele Identifier: CA1978930151

Gene: PYGM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64759941A= , CM000673.2:g.64759941A=	GRCh38
NC_000011.9:g.64527413A= , CM000673.1:g.64527413A=	GRCh37
NC_000011.8:g.64283989A=	NCBI36
NG_013018.1:g.5775T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000164139.4:c.-43T= MANE Select	ENSP00000164139.3:n.-43T=
ENST00000164139.3:c.-43T=	ENSP00000164139.3:n.-43T=
ENST00000377432.7:c.-43T=	ENSP00000366650.3:n.-43T=
NM_001164716.1:c.-43T=	NP_001158188.1:n.-43T=
NM_005609.2:c.-43T=	NP_005600.1:n.-43T=
NM_005609.3:c.-43T=	NP_005600.1:n.-43T=
NM_005609.4:c.-43T= MANE Select	NP_005600.1:n.-43T=