Canonical Allele Identifier: CA1428732431
Gene: CLDN1 HGNC NCBI
CLDN16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190322120C= , CM000665.2:g.190322120C= GRCh38
NC_000003.11:g.190039909C= , CM000665.1:g.190039909C= GRCh37
NC_000003.10:g.191522603C= NCBI36
NG_021418.1:g.5327G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295522.4:c.87G= (CLDN1) MANE Select ENSP00000295522.3:p.Gln29=
ENST00000295522.3:c.87G= (CLDN1) ENSP00000295522.3:p.Gln29=
NM_021101.4:c.87G= (CLDN1) NP_066924.1:p.Gln29=
NM_021101.5:c.87G= (CLDN1) MANE Select NP_066924.1:p.Gln29=
NM_001378492.1:c.-279+7061C= (CLDN16) NP_001365421.1:n.-279+7061C=
NM_001378493.1:c.-279+31529C= (CLDN16) NP_001365422.1:n.-279+31529C=