Canonical Allele Identifier: CA1428732558
Gene: CLDN1 HGNC NCBI
CLDN16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190322190_190322191delinsAG , CM000665.2:g.190322190_190322191delinsAG GRCh38
NC_000003.11:g.190039979_190039980delinsAG , CM000665.1:g.190039979_190039980delinsAG GRCh37
NC_000003.10:g.191522673_191522674delinsAG NCBI36
NG_021418.1:g.5256_5257delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000295522.4:c.16_17delinsCT (CLDN1) MANE Select ENSP00000295522.3:p.Leu6=
ENST00000295522.3:c.16_17delinsCT (CLDN1) ENSP00000295522.3:p.Leu6=
NM_021101.4:c.16_17delinsCT (CLDN1) NP_066924.1:p.Leu6=
NM_021101.5:c.16_17delinsCT (CLDN1) MANE Select NP_066924.1:p.Leu6=
NM_001378492.1:c.-279+7131_-279+7132delinsAG (CLDN16) NP_001365421.1:n.-279+7131_-279+7132delinsAG
NM_001378493.1:c.-279+31599_-279+31600delinsAG (CLDN16) NP_001365422.1:n.-279+31599_-279+31600delinsAG