Canonical Allele Identifier: CA1428732393
Gene: CLDN1 HGNC NCBI
CLDN16 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190322099G= , CM000665.2:g.190322099G= GRCh38
NC_000003.11:g.190039888G= , CM000665.1:g.190039888G= GRCh37
NC_000003.10:g.191522582G= NCBI36
NG_021418.1:g.5348C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295522.4:c.108C= (CLDN1) MANE Select ENSP00000295522.3:p.Ala36=
ENST00000295522.3:c.108C= (CLDN1) ENSP00000295522.3:p.Ala36=
NM_021101.4:c.108C= (CLDN1) NP_066924.1:p.Ala36=
NM_021101.5:c.108C= (CLDN1) MANE Select NP_066924.1:p.Ala36=
NM_001378492.1:c.-279+7040G= (CLDN16) NP_001365421.1:n.-279+7040G=
NM_001378493.1:c.-279+31508G= (CLDN16) NP_001365422.1:n.-279+31508G=
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