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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:
CA410196646
Gene: KCNE2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
2447577
ClinVar RCV Id:
RCV003176526
gnomAD v4:
21-34370679-C-G
MyVariant Identifiers:
chr21:g.35742978C>G (hg19)
chr21:g.34370679C>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000021.9:g.34370679C>G , CM000683.2:g.34370679C>G
GRCh38
NC_000021.8:g.35742978C>G , CM000683.1:g.35742978C>G
GRCh37
NC_000021.7:g.34664848C>G
NCBI36
NG_008804.1:g.11656C>G , LRG_291:g.11656C>G
Transcript Alleles
HGVS
Amino-acid change
ENST00000290310.4:c.201C>G
MANE Select
ENSP00000290310.2:p.Ile67Met
ENST00000290310.3:c.201C>G
ENSP00000290310.2:p.Ile67Met
NM_172201.1:c.201C>G , LRG_291t1:c.201C>G
NP_751951.1:p.Ile67Met
XR_937683.1:n.642G>C
XR_937684.1:n.642G>C
XR_001755012.2:n.763G>C
XR_001755013.2:n.642G>C
XR_937683.2:n.642G>C
NM_172201.2:c.201C>G
MANE Select
NP_751951.1:p.Ile67Met
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