Canonical Allele Identifier: CA381165482

Gene: PYGM

Linked Data

• MyVariant Identifiers: chr11:g.64514769T>A (hg19) ; chr11:g.64747297T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64747297T>A , CM000673.2:g.64747297T>A	GRCh38
NC_000011.9:g.64514769T>A , CM000673.1:g.64514769T>A	GRCh37
NC_000011.8:g.64271345T>A	NCBI36
NG_007574.1:g.3160A>T , LRG_100:g.3160A>T
NG_013018.1:g.18419A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000164139.4:c.2239A>T MANE Select	ENSP00000164139.3:p.Ser747Cys
ENST00000164139.3:c.2239A>T	ENSP00000164139.3:p.Ser747Cys
ENST00000377432.7:c.1975A>T	ENSP00000366650.3:p.Ser659Cys
ENST00000483742.1:n.1592A>T
NM_001164716.1:c.1975A>T	NP_001158188.1:p.Ser659Cys
NM_005609.2:c.2239A>T	NP_005600.1:p.Ser747Cys
NM_005609.3:c.2239A>T	NP_005600.1:p.Ser747Cys
NM_005609.4:c.2239A>T MANE Select	NP_005600.1:p.Ser747Cys