Canonical Allele Identifier: CA381164718

Gene: PYGM

Linked Data

• MyVariant Identifiers: chr11:g.64514458A>T (hg19) ; chr11:g.64746986A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64746986A>T , CM000673.2:g.64746986A>T	GRCh38
NC_000011.9:g.64514458A>T , CM000673.1:g.64514458A>T	GRCh37
NC_000011.8:g.64271034A>T	NCBI36
NG_007574.1:g.3471T>A , LRG_100:g.3471T>A
NG_013018.1:g.18730T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000164139.4:c.2314T>A MANE Select	ENSP00000164139.3:p.Phe772Ile
ENST00000164139.3:c.2314T>A	ENSP00000164139.3:p.Phe772Ile
ENST00000377432.7:c.2050T>A	ENSP00000366650.3:p.Phe684Ile
ENST00000483742.1:n.1667T>A
NM_001164716.1:c.2050T>A	NP_001158188.1:p.Phe684Ile
NM_005609.2:c.2314T>A	NP_005600.1:p.Phe772Ile
NM_005609.3:c.2314T>A	NP_005600.1:p.Phe772Ile
NM_005609.4:c.2314T>A MANE Select	NP_005600.1:p.Phe772Ile