Canonical Allele Identifier: CA637772699

Gene: CLDN14 CLDN14-AS1

Linked Data

• dbSNP Id: rs1169409606
• gnomAD v2: 21-37852070-T-G
• gnomAD v3: 21-36479772-T-G
• gnomAD v4: 21-36479772-T-G
• MyVariant Identifiers: chr21:g.37852070T>G (hg19) ; chr21:g.36479772T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.36479772T>G , CM000683.2:g.36479772T>G	GRCh38
NC_000021.8:g.37852070T>G , CM000683.1:g.37852070T>G	GRCh37
NC_000021.7:g.36773940T>G	NCBI36
NG_011777.1:g.101798A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000399135.6:c.-359A>C (CLDN14) MANE Select	ENSP00000382087.1:n.-359A>C
ENST00000342108.2:c.-81-17996A>C (CLDN14)	ENSP00000339292.2:n.-81-17996A>C
ENST00000399135.5:c.-359A>C (CLDN14)	ENSP00000382087.1:n.-359A>C
ENST00000399136.5:c.-81-17996A>C (CLDN14)	ENSP00000382088.1:n.-81-17996A>C
ENST00000399137.5:c.-549A>C (CLDN14)	ENSP00000382090.1:n.-549A>C
NM_001146077.1:c.-81-17996A>C (CLDN14)	NP_001139549.1:n.-81-17996A>C
NM_001146078.2:c.-81-17996A>C (CLDN14)	NP_001139550.1:n.-81-17996A>C
NM_001146079.1:c.-359A>C (CLDN14)	NP_001139551.1:n.-359A>C
NM_144492.2:c.-549A>C (CLDN14)	NP_652763.1:n.-549A>C
XM_011529519.1:c.-81-17996A>C (CLDN14)	XP_011527821.1:n.-81-17996A>C
XR_937694.1:n.962-459T>G (CLDN14-AS1)
XR_937695.1:n.469-459T>G (CLDN14-AS1)
XR_937696.1:n.853-459T>G (CLDN14-AS1)
XR_001755024.1:n.1022-459T>G (CLDN14-AS1)
XR_001755025.1:n.469-459T>G (CLDN14-AS1)
NM_001146079.2:c.-359A>C (CLDN14) MANE Select	NP_001139551.1:n.-359A>C
NM_001146078.3:c.-81-17996A>C (CLDN14)	NP_001139550.1:n.-81-17996A>C
NM_144492.3:c.-549A>C (CLDN14)	NP_652763.1:n.-549A>C
NM_001146077.2:c.-81-17996A>C (CLDN14)	NP_001139549.1:n.-81-17996A>C