Canonical Allele Identifier: CA2669053288
Gene: CLDN1 HGNC NCBI
CLDN16 HGNC NCBI

Linked Data

gnomAD v4: 3-190322243-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190322243A>G , CM000665.2:g.190322243A>G GRCh38
NC_000003.11:g.190040032A>G , CM000665.1:g.190040032A>G GRCh37
NC_000003.10:g.191522726A>G NCBI36
NG_021418.1:g.5204T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000295522.4:c.-37T>C (CLDN1) MANE Select ENSP00000295522.3:n.-37T>C
ENST00000295522.3:c.-37T>C (CLDN1) ENSP00000295522.3:n.-37T>C
NM_021101.4:c.-37T>C (CLDN1) NP_066924.1:n.-37T>C
NM_021101.5:c.-37T>C (CLDN1) MANE Select NP_066924.1:n.-37T>C
NM_001378492.1:c.-279+7184A>G (CLDN16) NP_001365421.1:n.-279+7184A>G
NM_001378493.1:c.-279+31652A>G (CLDN16) NP_001365422.1:n.-279+31652A>G
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