Canonical Allele Identifier: CA637772698

Gene: CLDN14 CLDN14-AS1

Linked Data

• dbSNP Id: rs1463618040
• gnomAD v2: 21-37852053-C-G
• gnomAD v3: 21-36479755-C-G
• gnomAD v4: 21-36479755-C-G
• MyVariant Identifiers: chr21:g.37852053C>G (hg19) ; chr21:g.36479755C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.36479755C>G , CM000683.2:g.36479755C>G	GRCh38
NC_000021.8:g.37852053C>G , CM000683.1:g.37852053C>G	GRCh37
NC_000021.7:g.36773923C>G	NCBI36
NG_011777.1:g.101815G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399135.6:c.-342G>C (CLDN14) MANE Select	ENSP00000382087.1:n.-342G>C
ENST00000342108.2:c.-81-17979G>C (CLDN14)	ENSP00000339292.2:n.-81-17979G>C
ENST00000399135.5:c.-342G>C (CLDN14)	ENSP00000382087.1:n.-342G>C
ENST00000399136.5:c.-81-17979G>C (CLDN14)	ENSP00000382088.1:n.-81-17979G>C
ENST00000399137.5:c.-532G>C (CLDN14)	ENSP00000382090.1:n.-532G>C
NM_001146077.1:c.-81-17979G>C (CLDN14)	NP_001139549.1:n.-81-17979G>C
NM_001146078.2:c.-81-17979G>C (CLDN14)	NP_001139550.1:n.-81-17979G>C
NM_001146079.1:c.-342G>C (CLDN14)	NP_001139551.1:n.-342G>C
NM_144492.2:c.-532G>C (CLDN14)	NP_652763.1:n.-532G>C
XM_011529519.1:c.-81-17979G>C (CLDN14)	XP_011527821.1:n.-81-17979G>C
XR_937694.1:n.962-476C>G (CLDN14-AS1)
XR_937695.1:n.469-476C>G (CLDN14-AS1)
XR_937696.1:n.853-476C>G (CLDN14-AS1)
XR_001755024.1:n.1022-476C>G (CLDN14-AS1)
XR_001755025.1:n.469-476C>G (CLDN14-AS1)
NM_001146079.2:c.-342G>C (CLDN14) MANE Select	NP_001139551.1:n.-342G>C
NM_001146078.3:c.-81-17979G>C (CLDN14)	NP_001139550.1:n.-81-17979G>C
NM_144492.3:c.-532G>C (CLDN14)	NP_652763.1:n.-532G>C
NM_001146077.2:c.-81-17979G>C (CLDN14)	NP_001139549.1:n.-81-17979G>C