Canonical Allele Identifier: CA1978919479

Gene: PYGM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64747359C= , CM000673.2:g.64747359C=	GRCh38
NC_000011.9:g.64514831C= , CM000673.1:g.64514831C=	GRCh37
NC_000011.8:g.64271407C=	NCBI36
NG_007574.1:g.3098G= , LRG_100:g.3098G=
NG_013018.1:g.18357G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000164139.4:c.2178-1G= MANE Select	ENSP00000164139.3:n.2178-1G=
ENST00000164139.3:c.2178-1G=	ENSP00000164139.3:n.2178-1G=
ENST00000377432.7:c.1914-1G=	ENSP00000366650.3:n.1914-1G=
ENST00000483742.1:n.1530G=
NM_001164716.1:c.1914-1G=	NP_001158188.1:n.1914-1G=
NM_005609.2:c.2178-1G=	NP_005600.1:n.2178-1G=
NM_005609.3:c.2178-1G=	NP_005600.1:n.2178-1G=
NM_005609.4:c.2178-1G= MANE Select	NP_005600.1:n.2178-1G=