Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.190322182A>G , CM000665.2:g.190322182A>G | GRCh38 |
| NC_000003.11:g.190039971A>G , CM000665.1:g.190039971A>G | GRCh37 |
| NC_000003.10:g.191522665A>G | NCBI36 |
| NG_021418.1:g.5265T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295522.4:c.25T>C (CLDN1) MANE Select | ENSP00000295522.3:p.Leu9= | |
| ENST00000295522.3:c.25T>C (CLDN1) | ENSP00000295522.3:p.Leu9= | |
| NM_021101.4:c.25T>C (CLDN1) | NP_066924.1:p.Leu9= | |
| NM_021101.5:c.25T>C (CLDN1) MANE Select | NP_066924.1:p.Leu9= | |
| NM_001378492.1:c.-279+7123A>G (CLDN16) | NP_001365421.1:n.-279+7123A>G | |
| NM_001378493.1:c.-279+31591A>G (CLDN16) | NP_001365422.1:n.-279+31591A>G |