Canonical Allele Identifier: CA381165614

Gene: PYGM

Linked Data

• MyVariant Identifiers: chr11:g.64514781T>G (hg19) ; chr11:g.64747309T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64747309T>G , CM000673.2:g.64747309T>G	GRCh38
NC_000011.9:g.64514781T>G , CM000673.1:g.64514781T>G	GRCh37
NC_000011.8:g.64271357T>G	NCBI36
NG_007574.1:g.3148A>C , LRG_100:g.3148A>C
NG_013018.1:g.18407A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000164139.4:c.2227A>C MANE Select	ENSP00000164139.3:p.Ile743Leu
ENST00000164139.3:c.2227A>C	ENSP00000164139.3:p.Ile743Leu
ENST00000377432.7:c.1963A>C	ENSP00000366650.3:p.Ile655Leu
ENST00000483742.1:n.1580A>C
NM_001164716.1:c.1963A>C	NP_001158188.1:p.Ile655Leu
NM_005609.2:c.2227A>C	NP_005600.1:p.Ile743Leu
NM_005609.3:c.2227A>C	NP_005600.1:p.Ile743Leu
NM_005609.4:c.2227A>C MANE Select	NP_005600.1:p.Ile743Leu