Canonical Allele Identifier: CA381165449

Gene: PYGM

Linked Data

• MyVariant Identifiers: chr11:g.64514765C>G (hg19) ; chr11:g.64747293C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64747293C>G , CM000673.2:g.64747293C>G	GRCh38
NC_000011.9:g.64514765C>G , CM000673.1:g.64514765C>G	GRCh37
NC_000011.8:g.64271341C>G	NCBI36
NG_007574.1:g.3164G>C , LRG_100:g.3164G>C
NG_013018.1:g.18423G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000164139.4:c.2243G>C MANE Select	ENSP00000164139.3:p.Ser748Thr
ENST00000164139.3:c.2243G>C	ENSP00000164139.3:p.Ser748Thr
ENST00000377432.7:c.1979G>C	ENSP00000366650.3:p.Ser660Thr
ENST00000483742.1:n.1596G>C
NM_001164716.1:c.1979G>C	NP_001158188.1:p.Ser660Thr
NM_005609.2:c.2243G>C	NP_005600.1:p.Ser748Thr
NM_005609.3:c.2243G>C	NP_005600.1:p.Ser748Thr
NM_005609.4:c.2243G>C MANE Select	NP_005600.1:p.Ser748Thr