Linked Data
gnomAD v4:
1-154571677-A-AT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.154571677_154571678insT , CM000663.2:g.154571677_154571678insT | GRCh38 |
| NC_000001.10:g.154544153_154544154insT , CM000663.1:g.154544153_154544154insT | GRCh37 |
| NC_000001.9:g.152810777_152810778insT | NCBI36 |
| NG_008027.1:g.8897_8898insT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368476.4:c.854_855insT MANE Select | ENSP00000357461.3:p.Lys285AsnfsTer? | |
| ENST00000636034.1:c.854_855insT | ENSP00000489703.1:p.Lys285AsnfsTer? | |
| ENST00000637900.1:c.860_861insT | ENSP00000490474.1:p.Lys287AsnfsTer? | |
| ENST00000368476.3:c.854_855insT | ENSP00000357461.3:p.Lys285AsnfsTer? | |
| NM_000748.2:c.854_855insT | NP_000739.1:p.Lys285AsnfsTer? | |
| XM_017000180.2:c.344_345insT | XP_016855669.1:p.Lys115AsnfsTer? | |
| XR_001736952.2:n.1106_1107insT | ||
| NM_000748.3:c.854_855insT MANE Select | NP_000739.1:p.Lys285AsnfsTer? |