Canonical Allele Identifier: CA381112078

Gene: PYGM

Linked Data

• MyVariant Identifiers: chr11:g.64527166T>A (hg19) ; chr11:g.64759694T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64759694T>A , CM000673.2:g.64759694T>A	GRCh38
NC_000011.9:g.64527166T>A , CM000673.1:g.64527166T>A	GRCh37
NC_000011.8:g.64283742T>A	NCBI36
NG_013018.1:g.6022A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000164139.4:c.205A>T MANE Select	ENSP00000164139.3:p.Ile69Phe
ENST00000164139.3:c.205A>T	ENSP00000164139.3:p.Ile69Phe
ENST00000377432.7:c.205A>T	ENSP00000366650.3:p.Ile69Phe
NM_001164716.1:c.205A>T	NP_001158188.1:p.Ile69Phe
NM_005609.2:c.205A>T	NP_005600.1:p.Ile69Phe
NM_005609.3:c.205A>T	NP_005600.1:p.Ile69Phe
NM_005609.4:c.205A>T MANE Select	NP_005600.1:p.Ile69Phe