Linked Data
dbSNP Id:
rs1313516899
gnomAD v2:
10-55566063-A-AAAAT
gnomAD v3:
10-53806303-A-AAAAT
gnomAD v4:
10-53806303-A-AAAAT
MyVariant Identifiers:
chr10:g.55566063_55566064insAAAT (hg19)
chr10:g.53806303_53806304insAAAT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.53806304_53806307dup , CM000672.2:g.53806304_53806307dup | GRCh38 |
| NC_000010.10:g.55566064_55566067dup , CM000672.1:g.55566064_55566067dup | GRCh37 |
| NC_000010.9:g.55236070_55236073dup | NCBI36 |
| NG_009191.2:g.999985_999988dup | |
| NG_009191.3:g.1827876_1827879dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644397.2:c.*272_*275dup MANE Select | ENSP00000495195.1:n.*272_*275dup | |
| ENST00000373965.6:c.*272_*275dup | ENSP00000363076.3:n.*272_*275dup | |
| ENST00000414778.5:c.*272_*275dup | ENSP00000410304.2:n.*272_*275dup | |
| ENST00000614895.4:c.*272_*275dup | ENSP00000478512.1:n.*272_*275dup | |
| ENST00000616114.4:c.*272_*275dup | ENSP00000483745.1:n.*272_*275dup | |
| NM_001142771.1:c.*272_*275dup | NP_001136243.1:n.*272_*275dup | |
| NM_001142772.1:c.*272_*275dup | NP_001136244.1:n.*272_*275dup | |
| NM_001354420.1:c.*272_*275dup | NP_001341349.1:n.*272_*275dup | |
| NM_001354429.1:c.*272_*275dup | NP_001341358.1:n.*272_*275dup | |
| XR_001747192.2:n.11787_11790dup | ||
| XR_001747193.2:n.11778_11781dup | ||
| NM_001142771.2:c.*272_*275dup | NP_001136243.1:n.*272_*275dup | |
| NM_001142772.2:c.*272_*275dup | NP_001136244.1:n.*272_*275dup | |
| NM_001354420.2:c.*272_*275dup | NP_001341349.1:n.*272_*275dup | |
| NM_001354429.2:c.*272_*275dup | NP_001341358.1:n.*272_*275dup | |
| NM_001384140.1:c.*272_*275dup MANE Select | NP_001371069.1:n.*272_*275dup |