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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:
CA405788689
Gene: DLL3
HGNC
NCBI
Linked Data
dbSNP Id:
rs1460780674
gnomAD v2:
19-39997997-A-G
gnomAD v3:
19-39507357-A-G
gnomAD v4:
19-39507357-A-G
MyVariant Identifiers:
chr19:g.39997997A>G (hg19)
chr19:g.39507357A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.39507357A>G , CM000681.2:g.39507357A>G
GRCh38
NC_000019.9:g.39997997A>G , CM000681.1:g.39997997A>G
GRCh37
NC_000019.8:g.44689837A>G
NCBI36
NG_008256.1:g.13441A>G
Transcript Alleles
HGVS
Amino-acid change
ENST00000356433.10:c.1412A>G
MANE Select
ENSP00000348810.4:p.Asp471Gly
ENST00000205143.4:c.1412A>G
ENSP00000205143.3:p.Asp471Gly
ENST00000356433.9:c.1412A>G
ENSP00000348810.4:p.Asp471Gly
NM_016941.3:c.1412A>G
NP_058637.1:p.Asp471Gly
NM_203486.2:c.1412A>G
NP_982353.1:p.Asp471Gly
NM_016941.4:c.1412A>G
NP_058637.1:p.Asp471Gly
NM_203486.3:c.1412A>G
MANE Select
NP_982353.1:p.Asp471Gly
Search 100 bp 5'
Search 100 bp 3'