Canonical Allele Identifier: CA1428735456
Gene: CLDN1 HGNC NCBI
CLDN16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190310253C= , CM000665.2:g.190310253C= GRCh38
NC_000003.11:g.190028042C= , CM000665.1:g.190028042C= GRCh37
NC_000003.10:g.191510736C= NCBI36
NG_021418.1:g.17194G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295522.4:c.389G= (CLDN1) MANE Select ENSP00000295522.3:p.Gly130=
ENST00000295522.3:c.389G= (CLDN1) ENSP00000295522.3:p.Gly130=
ENST00000490800.1:n.348G= (CLDN1)
NM_021101.4:c.389G= (CLDN1) NP_066924.1:p.Gly130=
XR_001741069.1:n.203-4640C=
NM_021101.5:c.389G= (CLDN1) MANE Select NP_066924.1:p.Gly130=
NM_001378492.1:c.-445-4640C= (CLDN16) NP_001365421.1:n.-445-4640C=
NM_001378493.1:c.-279+19662C= (CLDN16) NP_001365422.1:n.-279+19662C=