Linked Data
dbSNP Id:
rs770559996
gnomAD v2:
6-158535750-A-AGATAATACATTC
gnomAD v3:
6-158114718-A-AGATAATACATTC
gnomAD v4:
6-158114718-A-AGATAATACATTC
MyVariant Identifiers:
chr6:g.158535750_158535751insGATAATACATTC (hg19)
chr6:g.158114718_158114719insGATAATACATTC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.158114718_158114719insGATAATACATTC , CM000668.2:g.158114718_158114719insGATAATACATTC | GRCh38 |
| NC_000006.11:g.158535750_158535751insGATAATACATTC , CM000668.1:g.158535750_158535751insGATAATACATTC | GRCh37 |
| NC_000006.10:g.158455738_158455739insGATAATACATTC | NCBI36 |
| NG_032889.1:g.58562_58563insGAATGTATTATC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000607071.6:c.*1404+70_*1404+71insGAATGTATTATC | ENSP00000475855.1:n.*1404+70_*1404+71insGAATGTATTATC | |
| ENST00000642244.1:c.1594+70_1594+71insGAATGTATTATC | ENSP00000493554.1:n.1594+70_1594+71insGAATGTATTATC | |
| ENST00000642903.1:c.1754_1755insGAATGTATTATC | ENSP00000493559.1:p.Phe585delinsLeuAsnValLeuSer | |
| ENST00000644972.1:c.1684+70_1684+71insGAATGTATTATC | ENSP00000496451.1:n.1684+70_1684+71insGAATGTATTATC | |
| ENST00000645077.1:c.*1305+70_*1305+71insGAATGTATTATC | ENSP00000496113.1:n.*1305+70_*1305+71insGAATGTATTATC | |
| ENST00000645172.1:c.*1386+70_*1386+71insGAATGTATTATC | ENSP00000495367.1:n.*1386+70_*1386+71insGAATGTATTATC | |
| ENST00000646190.1:n.3015+70_3015+71insGAATGTATTATC | ||
| ENST00000646208.1:c.1420+70_1420+71insGAATGTATTATC | ENSP00000493723.1:n.1420+70_1420+71insGAATGTATTATC | |
| ENST00000646410.1:c.1555+70_1555+71insGAATGTATTATC | ENSP00000494205.1:n.1555+70_1555+71insGAATGTATTATC | |
| ENST00000646562.1:c.*1588_*1589insGAATGTATTATC | ENSP00000496087.1:n.*1588_*1589insGAATGTATTATC | |
| ENST00000647468.2:c.1684+70_1684+71insGAATGTATTATC MANE Select | ENSP00000496731.1:n.1684+70_1684+71insGAATGTATTATC | |
| ENST00000648111.1:c.*1372+70_*1372+71insGAATGTATTATC | ENSP00000497275.1:n.*1372+70_*1372+71insGAATGTATTATC | |
| ENST00000367104.7:c.1684+70_1684+71insGAATGTATTATC | ENSP00000356071.3:n.1684+70_1684+71insGAATGTATTATC | |
| ENST00000435180.5:c.479_480insGAATGTATTATC | ENSP00000391168.1:p.Phe160delinsLeuAsnValLeuSer | |
| ENST00000606965.5:c.*315_*316insGAATGTATTATC | ENSP00000475808.1:n.*315_*316insGAATGTATTATC | |
| ENST00000607071.5:c.*1618+70_*1618+71insGAATGTATTATC | ENSP00000475855.1:n.*1618+70_*1618+71insGAATGTATTATC | |
| ENST00000607742.5:c.*2962+70_*2962+71insGAATGTATTATC | ENSP00000475523.1:n.*2962+70_*2962+71insGAATGTATTATC | |
| NM_032861.3:c.1684+70_1684+71insGAATGTATTATC | NP_116250.3:n.1684+70_1684+71insGAATGTATTATC | |
| NR_073096.1:n.1687_1688insGAATGTATTATC | ||
| XM_006715586.1:c.1474+70_1474+71insGAATGTATTATC | XP_006715649.1:n.1474+70_1474+71insGAATGTATTATC | |
| XM_011536196.1:c.1663+70_1663+71insGAATGTATTATC | XP_011534498.1:n.1663+70_1663+71insGAATGTATTATC | |
| XM_011536197.1:c.1570+70_1570+71insGAATGTATTATC | XP_011534499.1:n.1570+70_1570+71insGAATGTATTATC | |
| XM_011536198.1:c.1474+70_1474+71insGAATGTATTATC | XP_011534500.1:n.1474+70_1474+71insGAATGTATTATC | |
| XM_006715586.3:c.1474+70_1474+71insGAATGTATTATC | XP_006715649.1:n.1474+70_1474+71insGAATGTATTATC | |
| XM_011536196.3:c.1663+70_1663+71insGAATGTATTATC | XP_011534498.1:n.1663+70_1663+71insGAATGTATTATC | |
| XM_011536198.3:c.1474+70_1474+71insGAATGTATTATC | XP_011534500.1:n.1474+70_1474+71insGAATGTATTATC | |
| XM_024446573.1:c.1684+70_1684+71insGAATGTATTATC | XP_024302341.1:n.1684+70_1684+71insGAATGTATTATC | |
| XR_001743697.2:n.1715+70_1715+71insGAATGTATTATC | ||
| XR_942606.2:n.1766+70_1766+71insGAATGTATTATC | ||
| NM_032861.4:c.1684+70_1684+71insGAATGTATTATC MANE Select | NP_116250.3:n.1684+70_1684+71insGAATGTATTATC | |
| NR_073096.2:n.1669_1670insGAATGTATTATC |