Canonical Allele Identifier: CA355758602
Gene: CLDN1 HGNC NCBI
CLDN16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.190039917G>C (hg19) chr3:g.190322128G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190322128G>C , CM000665.2:g.190322128G>C GRCh38
NC_000003.11:g.190039917G>C , CM000665.1:g.190039917G>C GRCh37
NC_000003.10:g.191522611G>C NCBI36
NG_021418.1:g.5319C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295522.4:c.79C>G (CLDN1) MANE Select ENSP00000295522.3:p.Leu27Val
ENST00000295522.3:c.79C>G (CLDN1) ENSP00000295522.3:p.Leu27Val
NM_021101.4:c.79C>G (CLDN1) NP_066924.1:p.Leu27Val
NM_021101.5:c.79C>G (CLDN1) MANE Select NP_066924.1:p.Leu27Val
NM_001378492.1:c.-279+7069G>C (CLDN16) NP_001365421.1:n.-279+7069G>C
NM_001378493.1:c.-279+31537G>C (CLDN16) NP_001365422.1:n.-279+31537G>C
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