Linked Data
MyVariant Identifiers:
chr3:g.190027969T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.190310180T>C , CM000665.2:g.190310180T>C | GRCh38 |
| NC_000003.11:g.190027969T>C , CM000665.1:g.190027969T>C | GRCh37 |
| NC_000003.10:g.191510663T>C | NCBI36 |
| NG_021418.1:g.17267A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295522.4:c.462A>G (CLDN1) MANE Select | ENSP00000295522.3:p.Pro154= | |
| ENST00000295522.3:c.462A>G (CLDN1) | ENSP00000295522.3:p.Pro154= | |
| ENST00000490800.1:n.421A>G (CLDN1) | ||
| NM_021101.4:c.462A>G (CLDN1) | NP_066924.1:p.Pro154= | |
| XR_001741069.1:n.203-4713T>C | ||
| NM_021101.5:c.462A>G (CLDN1) MANE Select | NP_066924.1:p.Pro154= | |
| NM_001378492.1:c.-445-4713T>C (CLDN16) | NP_001365421.1:n.-445-4713T>C | |
| NM_001378493.1:c.-279+19589T>C (CLDN16) | NP_001365422.1:n.-279+19589T>C |