Canonical Allele Identifier: CA1978920756

Gene: PYGM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64753381G= , CM000673.2:g.64753381G=	GRCh38
NC_000011.9:g.64520853G= , CM000673.1:g.64520853G=	GRCh37
NC_000011.8:g.64277429G=	NCBI36
NG_013018.1:g.12335C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000164139.4:c.1403+138C= MANE Select	ENSP00000164139.3:n.1403+138C=
ENST00000164139.3:c.1403+138C=	ENSP00000164139.3:n.1403+138C=
ENST00000377432.7:c.1139+138C=	ENSP00000366650.3:n.1139+138C=
NM_001164716.1:c.1139+138C=	NP_001158188.1:n.1139+138C=
NM_005609.2:c.1403+138C=	NP_005600.1:n.1403+138C=
NM_005609.3:c.1403+138C=	NP_005600.1:n.1403+138C=
NM_005609.4:c.1403+138C= MANE Select	NP_005600.1:n.1403+138C=