Canonical Allele Identifier: CA2388025732
Gene: CLDN14 HGNC NCBI
CLDN14-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1601601071

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.36479752T>G , CM000683.2:g.36479752T>G GRCh38
NC_000021.8:g.37852050T>G , CM000683.1:g.37852050T>G GRCh37
NC_000021.7:g.36773920T>G NCBI36
NG_011777.1:g.101818A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000399135.6:c.-339A>C (CLDN14) MANE Select ENSP00000382087.1:n.-339A>C
ENST00000342108.2:c.-81-17976A>C (CLDN14) ENSP00000339292.2:n.-81-17976A>C
ENST00000399135.5:c.-339A>C (CLDN14) ENSP00000382087.1:n.-339A>C
ENST00000399136.5:c.-81-17976A>C (CLDN14) ENSP00000382088.1:n.-81-17976A>C
ENST00000399137.5:c.-529A>C (CLDN14) ENSP00000382090.1:n.-529A>C
NM_001146077.1:c.-81-17976A>C (CLDN14) NP_001139549.1:n.-81-17976A>C
NM_001146078.2:c.-81-17976A>C (CLDN14) NP_001139550.1:n.-81-17976A>C
NM_001146079.1:c.-339A>C (CLDN14) NP_001139551.1:n.-339A>C
NM_144492.2:c.-529A>C (CLDN14) NP_652763.1:n.-529A>C
XM_011529519.1:c.-81-17976A>C (CLDN14) XP_011527821.1:n.-81-17976A>C
XR_937694.1:n.962-479T>G (CLDN14-AS1)
XR_937695.1:n.469-479T>G (CLDN14-AS1)
XR_937696.1:n.853-479T>G (CLDN14-AS1)
XR_001755024.1:n.1022-479T>G (CLDN14-AS1)
XR_001755025.1:n.469-479T>G (CLDN14-AS1)
NM_001146079.2:c.-339A>C (CLDN14) MANE Select NP_001139551.1:n.-339A>C
NM_001146078.3:c.-81-17976A>C (CLDN14) NP_001139550.1:n.-81-17976A>C
NM_144492.3:c.-529A>C (CLDN14) NP_652763.1:n.-529A>C
NM_001146077.2:c.-81-17976A>C (CLDN14) NP_001139549.1:n.-81-17976A>C