Canonical Allele Identifier: CA749044436
Gene: CLDN14 HGNC NCBI
CLDN14-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1360193462
MyVariant Identifiers: chr21:g.37851982A>C (hg19) chr21:g.36479684A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.36479684A>C , CM000683.2:g.36479684A>C GRCh38
NC_000021.8:g.37851982A>C , CM000683.1:g.37851982A>C GRCh37
NC_000021.7:g.36773852A>C NCBI36
NG_011777.1:g.101886T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000399135.6:c.-271T>G (CLDN14) MANE Select ENSP00000382087.1:n.-271T>G
ENST00000342108.2:c.-81-17908T>G (CLDN14) ENSP00000339292.2:n.-81-17908T>G
ENST00000399135.5:c.-271T>G (CLDN14) ENSP00000382087.1:n.-271T>G
ENST00000399136.5:c.-81-17908T>G (CLDN14) ENSP00000382088.1:n.-81-17908T>G
ENST00000399137.5:c.-461T>G (CLDN14) ENSP00000382090.1:n.-461T>G
NM_001146077.1:c.-81-17908T>G (CLDN14) NP_001139549.1:n.-81-17908T>G
NM_001146078.2:c.-81-17908T>G (CLDN14) NP_001139550.1:n.-81-17908T>G
NM_001146079.1:c.-271T>G (CLDN14) NP_001139551.1:n.-271T>G
NM_144492.2:c.-461T>G (CLDN14) NP_652763.1:n.-461T>G
XM_011529519.1:c.-81-17908T>G (CLDN14) XP_011527821.1:n.-81-17908T>G
XR_937694.1:n.962-547A>C (CLDN14-AS1)
XR_937695.1:n.469-547A>C (CLDN14-AS1)
XR_937696.1:n.853-547A>C (CLDN14-AS1)
XR_001755024.1:n.1022-547A>C (CLDN14-AS1)
XR_001755025.1:n.469-547A>C (CLDN14-AS1)
NM_001146079.2:c.-271T>G (CLDN14) MANE Select NP_001139551.1:n.-271T>G
NM_001146078.3:c.-81-17908T>G (CLDN14) NP_001139550.1:n.-81-17908T>G
NM_144492.3:c.-461T>G (CLDN14) NP_652763.1:n.-461T>G
NM_001146077.2:c.-81-17908T>G (CLDN14) NP_001139549.1:n.-81-17908T>G
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