Canonical Allele Identifier: CA2840305681

Gene: PYGM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64758422G>T , CM000673.2:g.64758422G>T	GRCh38
NC_000011.9:g.64525894G>T , CM000673.1:g.64525894G>T	GRCh37
NC_000011.8:g.64282470G>T	NCBI36
NG_013018.1:g.7294C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000164139.4:c.424+15C>A MANE Select	ENSP00000164139.3:n.424+15C>A
ENST00000164139.3:c.424+15C>A	ENSP00000164139.3:n.424+15C>A
ENST00000377432.7:c.244-156C>A	ENSP00000366650.3:n.244-156C>A
NM_001164716.1:c.244-156C>A	NP_001158188.1:n.244-156C>A
NM_005609.2:c.424+15C>A	NP_005600.1:n.424+15C>A
NM_005609.3:c.424+15C>A	NP_005600.1:n.424+15C>A
NM_005609.4:c.424+15C>A MANE Select	NP_005600.1:n.424+15C>A