WARNING - Protein Allele ID and Protein Sequence HGVS API Requests Temporarily Disabled:
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.
Linked Data
ClinVar Variation Id:
555639
ClinVar RCV Id:
RCV000671497
dbSNP Id:
rs1553857901
gnomAD v4:
4-5711448-C-CGGCGCCCGCCCTGCT
MyVariant Identifiers:
chr4:g.5711452_5711466dup (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.5711452_5711466dup , CM000666.2:g.5711452_5711466dup | GRCh38 |
| NC_000004.11:g.5713179_5713193dup , CM000666.1:g.5713179_5713193dup | GRCh37 |
| NC_000004.10:g.5764080_5764094dup | NCBI36 |
| NG_008843.1:g.5256_5270dup | |
| NG_015821.1:g.3086_3100dup |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000264956.11:c.72_86dup MANE Select | ENSP00000264956.6:p.Ala29_Pro30insProAlaL... | |
| ENST00000264956.10:c.72_86dup | ENSP00000264956.6:p.Ala29_Pro30insProAlaL... | |
| ENST00000509451.1:c.72_86dup | ENSP00000426774.1:p.Ala29_Pro30insProAlaL... | |
| NM_001306090.1:c.72_86dup | NP_001293019.1:p.Ala29_Pro30insProAlaLeuL... | |
| NM_001306092.1:c.72_86dup | NP_001293021.1:p.Ala29_Pro30insProAlaLeuL... | |
| NM_153717.2:c.72_86dup | NP_714928.1:p.Ala29_Pro30insProAlaLeuLeuA... | |
| XM_006713865.2:c.72_86dup | XP_006713928.1:p.Ala29_Pro30insProAlaLeuL... | |
| XM_006713866.2:c.72_86dup | XP_006713929.1:p.Ala29_Pro30insProAlaLeuL... | |
| XM_011513419.1:c.72_86dup | XP_011511721.1:p.Ala29_Pro30insProAlaLeuL... | |
| XR_427473.2:n.262_276dup | ||
| XR_427475.2:n.262_276dup | ||
| XR_427476.2:n.262_276dup | ||
| XR_924920.1:n.262_276dup | ||
| XR_924921.1:n.262_276dup | ||
| XR_924922.1:n.262_276dup | ||
| XR_924923.1:n.262_276dup | ||
| XR_924924.1:n.262_276dup | ||
| XR_924925.1:n.262_276dup | ||
| XR_924926.1:n.262_276dup | ||
| XR_924927.1:n.262_276dup | ||
| XR_924928.1:n.264_278dup | ||
| XM_006713865.3:c.72_86dup | XP_006713928.1:p.Ala29_Pro30insProAlaLeuL... | |
| XM_006713866.3:c.72_86dup | XP_006713929.1:p.Ala29_Pro30insProAlaLeuL... | |
| XM_011513419.2:c.72_86dup | XP_011511721.1:p.Ala29_Pro30insProAlaLeuL... | |
| XM_017007883.2:c.72_86dup | XP_016863372.1:p.Ala29_Pro30insProAlaLeuL... | |
| XR_001741164.1:n.252_266dup | ||
| XR_001741165.1:n.252_266dup | ||
| XR_001741166.1:n.252_266dup | ||
| XR_001741167.1:n.252_266dup | ||
| XR_001741168.1:n.252_266dup | ||
| XR_001741169.2:n.254_268dup | ||
| XR_001741170.1:n.254_268dup | ||
| XR_427473.3:n.252_266dup | ||
| XR_427475.3:n.252_266dup | ||
| XR_427476.3:n.252_266dup | ||
| XR_924920.2:n.252_266dup | ||
| XR_924921.2:n.252_266dup | ||
| XR_924922.2:n.252_266dup | ||
| XR_924924.2:n.252_266dup | ||
| XR_924925.2:n.252_266dup | ||
| XR_924926.2:n.252_266dup | ||
| NM_153717.3:c.72_86dup MANE Select | NP_714928.1:p.Ala29_Pro30insProAlaLeuLeuA... | |
| NM_001306090.2:c.72_86dup | NP_001293019.1:p.Ala29_Pro30insProAlaLeuL... | |
| NM_001306092.2:c.72_86dup | NP_001293021.1:p.Ala29_Pro30insProAlaLeuL... |