Canonical Allele Identifier: CA474958582

Gene: PYGM

Linked Data

• MyVariant Identifiers: chr11:g.64514752G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64747280G>T , CM000673.2:g.64747280G>T	GRCh38
NC_000011.9:g.64514752G>T , CM000673.1:g.64514752G>T	GRCh37
NC_000011.8:g.64271328G>T	NCBI36
NG_007574.1:g.3177C>A , LRG_100:g.3177C>A
NG_013018.1:g.18436C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000164139.4:c.2256C>A MANE Select	ENSP00000164139.3:p.Ser752=
ENST00000164139.3:c.2256C>A	ENSP00000164139.3:p.Ser752=
ENST00000377432.7:c.1992C>A	ENSP00000366650.3:p.Ser664=
ENST00000483742.1:n.1609C>A
NM_001164716.1:c.1992C>A	NP_001158188.1:p.Ser664=
NM_005609.2:c.2256C>A	NP_005600.1:p.Ser752=
NM_005609.3:c.2256C>A	NP_005600.1:p.Ser752=
NM_005609.4:c.2256C>A MANE Select	NP_005600.1:p.Ser752=