Linked Data
dbSNP Id:
rs1441699354
gnomAD v2:
6-10556249-A-ATTCTCG
gnomAD v3:
6-10556016-A-ATTCTCG
gnomAD v4:
6-10556016-A-ATTCTCG
MyVariant Identifiers:
chr6:g.10556249_10556250insTTCTCG (hg19)
chr6:g.10556016_10556017insTTCTCG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.10556019_10556020insTCGTTC , CM000668.2:g.10556019_10556020insTCGTTC | GRCh38 |
| NC_000006.11:g.10556252_10556253insTCGTTC , CM000668.1:g.10556252_10556253insTCGTTC | GRCh37 |
| NC_000006.10:g.10664238_10664239insTCGTTC | NCBI36 |
| NG_007469.3:g.68797_68798insTCGTTC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000316170.9:c.-405_-404insTCGTTC MANE Plus Clinical | ENSP00000314844.3:n.-405_-404insTCGTTC | |
| ENST00000397423.7:n.484+27178_484+27179insTCGTTC | ||
| ENST00000495262.7:c.925+26183_925+26184insTCGTTC MANE Select | ENSP00000419411.2:n.925+26183_925+26184insTCGTTC | |
| ENST00000316170.7:c.-405_-404insTCGTTC | ENSP00000314844.3:n.-405_-404insTCGTTC | |
| ENST00000379597.7:c.925+26183_925+26184insTCGTTC | ENSP00000368917.3:n.925+26183_925+26184insTCGTTC | |
| ENST00000397423.6:n.484+27178_484+27179insTCGTTC | ||
| ENST00000410107.5:c.67+46861_67+46862insTCGTTC | ENSP00000386321.1:n.67+46861_67+46862insTCGTTC | |
| ENST00000461400.1:n.25+26183_25+26184insTCGTTC | ||
| ENST00000474518.1:n.508+27178_508+27179insTCGTTC | ||
| ENST00000475577.5:n.254+28359_254+28360insTCGTTC | ||
| ENST00000485764.1:n.40+26183_40+26184insTCGTTC | ||
| ENST00000489225.5:n.283+63088_283+63089insTCGTTC | ||
| ENST00000489819.5:n.175+34425_175+34426insTCGTTC | ||
| ENST00000495262.5:c.925+26183_925+26184insTCGTTC | ENSP00000419411.1:n.925+26183_925+26184insTCGTTC | |
| NM_001491.2:c.-405_-404insTCGTTC | NP_001482.1:n.-405_-404insTCGTTC | |
| NM_145649.4:c.925+26183_925+26184insTCGTTC | NP_663624.1:n.925+26183_925+26184insTCGTTC | |
| XM_005248997.2:c.-405_-404insTCGTTC | XP_005249054.1:n.-405_-404insTCGTTC | |
| XM_005248999.2:c.694+26183_694+26184insTCGTTC | XP_005249056.1:n.694+26183_694+26184insTCGTTC | |
| XM_006715052.2:c.925+26183_925+26184insTCGTTC | XP_006715115.1:n.925+26183_925+26184insTCGTTC | |
| XM_006715053.2:c.*61_*62insTCGTTC | XP_006715116.1:n.*61_*62insTCGTTC | |
| XM_011514465.1:c.926-17111_926-17110insTCGTTC | XP_011512767.1:n.926-17111_926-17110insTCGTTC | |
| XM_011514467.1:c.694+26183_694+26184insTCGTTC | XP_011512769.1:n.694+26183_694+26184insTCGTTC | |
| XR_926136.1:n.1476+26183_1476+26184insTCGTTC | ||
| XM_005248997.3:c.-405_-404insTCGTTC | XP_005249054.1:n.-405_-404insTCGTTC | |
| XM_006715052.3:c.925+26183_925+26184insTCGTTC | XP_006715115.1:n.925+26183_925+26184insTCGTTC | |
| XR_002956275.1:n.1476+26183_1476+26184insTCGTTC | ||
| XR_926136.2:n.1474+26183_1474+26184insTCGTTC | ||
| NM_001374747.1:c.925+26183_925+26184insTCGTTC | NP_001361676.1:n.925+26183_925+26184insTCGTTC | |
| NM_001491.3:c.-405_-404insTCGTTC MANE Plus Clinical | NP_001482.1:n.-405_-404insTCGTTC | |
| NM_145649.5:c.925+26183_925+26184insTCGTTC MANE Select | NP_663624.1:n.925+26183_925+26184insTCGTTC |