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:
551530
ClinVar RCV Id:
RCV000666612
dbSNP Id:
rs1555598880
MyVariant Identifiers:
chr17:g.80105034dup (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.80105034dup , CM000679.2:g.80105034dup | GRCh38 |
| NC_000017.10:g.78078833dup , CM000679.1:g.78078833dup | GRCh37 |
| NC_000017.9:g.75693428dup | NCBI36 |
| NG_009822.1:g.8479dup , LRG_673:g.8479dup |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000570803.6:c.448dup | ENSP00000460543.2:p.Ala150GlyfsTer27 | |
| ENST00000572080.2:c.448dup | ENSP00000459972.2:p.Ala150GlyfsTer27 | |
| ENST00000577106.6:c.448dup | ENSP00000458306.2:p.Ala150GlyfsTer27 | |
| ENST00000302262.8:c.448dup MANE Select | ENSP00000305692.3:p.Ala150GlyfsTer27 | |
| ENST00000302262.7:c.448dup | ENSP00000305692.3:p.Ala150GlyfsTer27 | |
| ENST00000390015.7:c.448dup | ENSP00000374665.3:p.Ala150GlyfsTer27 | |
| ENST00000570803.5:c.448dup | ENSP00000460543.1:p.Ala150GlyfsTer27 | |
| ENST00000577106.5:c.448dup | ENSP00000458306.1:p.Ala150GlyfsTer27 | |
| NM_000152.3:c.448dup , LRG_673t1:c.448dup | NP_000143.2:p.Ala150GlyfsTer27 | |
| NM_001079803.1:c.448dup | NP_001073271.1:p.Ala150GlyfsTer27 | |
| NM_001079804.1:c.448dup | NP_001073272.1:p.Ala150GlyfsTer27 | |
| XM_005257193.1:c.448dup | XP_005257250.1:p.Ala150GlyfsTer27 | |
| XM_005257194.3:c.448dup | XP_005257251.1:p.Ala150GlyfsTer27 | |
| NM_000152.4:c.448dup | NP_000143.2:p.Ala150GlyfsTer27 | |
| NM_001079803.2:c.448dup | NP_001073271.1:p.Ala150GlyfsTer27 | |
| NM_001079804.2:c.448dup | NP_001073272.1:p.Ala150GlyfsTer27 | |
| XM_005257193.2:c.448dup | XP_005257250.1:p.Ala150GlyfsTer27 | |
| XM_005257194.4:c.448dup | XP_005257251.1:p.Ala150GlyfsTer27 | |
| NM_000152.5:c.448dup MANE Select | NP_000143.2:p.Ala150GlyfsTer27 | |
| NM_001079803.3:c.448dup | NP_001073271.1:p.Ala150GlyfsTer27 | |
| NM_001079804.3:c.448dup | NP_001073272.1:p.Ala150GlyfsTer27 |