Canonical Allele Identifier: CA1978919802

Gene: PYGM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64747492C= , CM000673.2:g.64747492C=	GRCh38
NC_000011.9:g.64514964C= , CM000673.1:g.64514964C=	GRCh37
NC_000011.8:g.64271540C=	NCBI36
NG_007574.1:g.2965G= , LRG_100:g.2965G=
NG_013018.1:g.18224G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000164139.4:c.2178-134G= MANE Select	ENSP00000164139.3:n.2178-134G=
ENST00000164139.3:c.2178-134G=	ENSP00000164139.3:n.2178-134G=
ENST00000377432.7:c.1914-134G=	ENSP00000366650.3:n.1914-134G=
ENST00000483742.1:n.1397G=
NM_001164716.1:c.1914-134G=	NP_001158188.1:n.1914-134G=
NM_005609.2:c.2178-134G=	NP_005600.1:n.2178-134G=
NM_005609.3:c.2178-134G=	NP_005600.1:n.2178-134G=
NM_005609.4:c.2178-134G= MANE Select	NP_005600.1:n.2178-134G=