Canonical Allele Identifier: CA381165518

Gene: PYGM

Linked Data

• MyVariant Identifiers: chr11:g.64514772G>T (hg19) ; chr11:g.64747300G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64747300G>T , CM000673.2:g.64747300G>T	GRCh38
NC_000011.9:g.64514772G>T , CM000673.1:g.64514772G>T	GRCh37
NC_000011.8:g.64271348G>T	NCBI36
NG_007574.1:g.3157C>A , LRG_100:g.3157C>A
NG_013018.1:g.18416C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000164139.4:c.2236C>A MANE Select	ENSP00000164139.3:p.Leu746Met
ENST00000164139.3:c.2236C>A	ENSP00000164139.3:p.Leu746Met
ENST00000377432.7:c.1972C>A	ENSP00000366650.3:p.Leu658Met
ENST00000483742.1:n.1589C>A
NM_001164716.1:c.1972C>A	NP_001158188.1:p.Leu658Met
NM_005609.2:c.2236C>A	NP_005600.1:p.Leu746Met
NM_005609.3:c.2236C>A	NP_005600.1:p.Leu746Met
NM_005609.4:c.2236C>A MANE Select	NP_005600.1:p.Leu746Met