Linked Data
dbSNP Id:
rs1349522517
MyVariant Identifiers:
chr16:g.30997832_30997833insACCTTCT (hg19)
chr16:g.30986511_30986512insACCTTCT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.30986512_30986513insCCTTCTA , CM000678.2:g.30986512_30986513insCCTTCTA | GRCh38 |
| NC_000016.9:g.30997833_30997834insCCTTCTA , CM000678.1:g.30997833_30997834insCCTTCTA | GRCh37 |
| NC_000016.8:g.30905334_30905335insCCTTCTA | NCBI36 |
| NG_012346.1:g.6315_6316insCCTTCTA | |
| NG_052948.1:g.34219_34220insCCTTCTA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297679.10:c.412_413insCCTTCTA MANE Select | ENSP00000297679.5:p.Lys138ThrfsTer3 | |
| ENST00000262520.10:c.412_413insCCTTCTA | ENSP00000262520.6:p.Lys138ThrfsTer3 | |
| ENST00000297679.9:c.412_413insCCTTCTA | ENSP00000297679.5:p.Lys138ThrfsTer3 | |
| ENST00000562932.5:c.535_536insCCTTCTA | ENSP00000459852.1:p.Lys179ThrfsTer3 | |
| ENST00000574447.1:c.412_413insCCTTCTA | ENSP00000459689.1:p.Lys138ThrfsTer3 | |
| NM_001142777.1:c.412_413insCCTTCTA | NP_001136249.1:p.Lys138ThrfsTer3 | |
| NM_001142778.1:c.412_413insCCTTCTA | NP_001136250.1:p.Lys138ThrfsTer3 | |
| NM_025193.3:c.412_413insCCTTCTA | NP_079469.2:p.Lys138ThrfsTer3 | |
| XM_005255601.3:c.412_413insCCTTCTA | XP_005255658.2:p.Lys138ThrfsTer3 | |
| XM_011545960.1:c.412_413insCCTTCTA | XP_011544262.1:p.Lys138ThrfsTer3 | |
| XM_011545961.1:c.412_413insCCTTCTA | XP_011544263.1:p.Lys138ThrfsTer3 | |
| XM_011545962.1:c.412_413insCCTTCTA | XP_011544264.1:p.Lys138ThrfsTer3 | |
| XM_011545960.2:c.412_413insCCTTCTA | XP_011544262.1:p.Lys138ThrfsTer3 | |
| XM_011545962.2:c.412_413insCCTTCTA | XP_011544264.1:p.Lys138ThrfsTer3 | |
| XM_017023732.1:c.412_413insCCTTCTA | XP_016879221.1:p.Lys138ThrfsTer3 | |
| NM_025193.4:c.412_413insCCTTCTA MANE Select | NP_079469.2:p.Lys138ThrfsTer3 | |
| NM_001142777.2:c.412_413insCCTTCTA | NP_001136249.1:p.Lys138ThrfsTer3 | |
| NM_001142778.2:c.412_413insCCTTCTA | NP_001136250.1:p.Lys138ThrfsTer3 |