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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:
CA414410216
Gene: GLUD2
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chrX:g.120182259G>C (hg19)
chrX:g.121048405G>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.121048405G>C , CM000685.2:g.121048405G>C
GRCh38
NC_000023.10:g.120182259G>C , CM000685.1:g.120182259G>C
GRCh37
NC_000023.9:g.120009940G>C
NCBI36
NG_016456.1:g.5798G>C
Transcript Alleles
HGVS
Amino-acid change
ENST00000328078.3:c.721G>C
MANE Select
ENSP00000327589.1:p.Ala241Pro
ENST00000328078.2:c.721G>C
ENSP00000327589.1:p.Ala241Pro
NM_012084.3:c.721G>C
NP_036216.2:p.Ala241Pro
NM_012084.4:c.721G>C
MANE Select
NP_036216.2:p.Ala241Pro
Search 100 bp 5'
Search 100 bp 3'