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UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
CA381167580
Gene: PYGM
HGNC
NCBI
Linked Data
COSMIC:
COSM390458
MyVariant Identifiers:
chr11:g.64517892G>C (hg19)
chr11:g.64750420G>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.64750420G>C , CM000673.2:g.64750420G>C
GRCh38
NC_000011.9:g.64517892G>C , CM000673.1:g.64517892G>C
GRCh37
NC_000011.8:g.64274468G>C
NCBI36
NG_007574.1:g.37C>G , LRG_100:g.37C>G
NG_013018.1:g.15296C>G
Transcript Alleles
HGVS
Amino-acid change
ENST00000164139.4:c.2133C>G
MANE Select
ENSP00000164139.3:p.Ile711Met
ENST00000164139.3:c.2133C>G
ENSP00000164139.3:p.Ile711Met
ENST00000377432.7:c.1869C>G
ENSP00000366650.3:p.Ile623Met
NM_001164716.1:c.1869C>G
NP_001158188.1:p.Ile623Met
NM_005609.2:c.2133C>G
NP_005600.1:p.Ile711Met
NM_005609.3:c.2133C>G
NP_005600.1:p.Ile711Met
NM_005609.4:c.2133C>G
MANE Select
NP_005600.1:p.Ile711Met
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