Canonical Allele Identifier: CA10019183

Gene: CLDN14 CLDN14-AS1

Linked Data

• ClinVar Variation Id: 339885
• ClinVar RCV Id: RCV000276784 ; RCV001597106
• dbSNP Id: rs114551506
• ExAC: 21:37833223 C / T
• gnomAD v2: 21-37833223-C-T
• gnomAD v3: 21-36460925-C-T
• gnomAD v4: 21-36460925-C-T
• MyVariant Identifiers: chr21:g.37833223C>T (hg19) ; chr21:g.36460925C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.36460925C>T , CM000683.2:g.36460925C>T	GRCh38
NC_000021.8:g.37833223C>T , CM000683.1:g.37833223C>T	GRCh37
NC_000021.7:g.36755093C>T	NCBI36
NG_011777.1:g.120645G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399135.6:c.*51G>A (CLDN14) MANE Select	ENSP00000382087.1:n.*51G>A
ENST00000342108.2:c.*51G>A (CLDN14)	ENSP00000339292.2:n.*51G>A
ENST00000399135.5:c.*51G>A (CLDN14)	ENSP00000382087.1:n.*51G>A
ENST00000399136.5:c.*51G>A (CLDN14)	ENSP00000382088.1:n.*51G>A
ENST00000399137.5:c.*51G>A (CLDN14)	ENSP00000382090.1:n.*51G>A
ENST00000399139.5:c.*51G>A (CLDN14)	ENSP00000382092.1:n.*51G>A
NM_001146077.1:c.*51G>A (CLDN14)	NP_001139549.1:n.*51G>A
NM_001146078.2:c.*51G>A (CLDN14)	NP_001139550.1:n.*51G>A
NM_001146079.1:c.*51G>A (CLDN14)	NP_001139551.1:n.*51G>A
NM_012130.3:c.*51G>A (CLDN14)	NP_036262.1:n.*51G>A
NM_144492.2:c.*51G>A (CLDN14)	NP_652763.1:n.*51G>A
XM_011529519.1:c.*51G>A (CLDN14)	XP_011527821.1:n.*51G>A
XR_937694.1:n.468+14918C>T (CLDN14-AS1)
XR_937695.1:n.468+14918C>T (CLDN14-AS1)
XR_937696.1:n.468+14918C>T (CLDN14-AS1)
XR_001755025.1:n.468+14918C>T (CLDN14-AS1)
NM_001146079.2:c.*51G>A (CLDN14) MANE Select	NP_001139551.1:n.*51G>A
NM_001146078.3:c.*51G>A (CLDN14)	NP_001139550.1:n.*51G>A
NM_012130.4:c.*51G>A (CLDN14)	NP_036262.1:n.*51G>A
NM_144492.3:c.*51G>A (CLDN14)	NP_652763.1:n.*51G>A
NM_001146077.2:c.*51G>A (CLDN14)	NP_001139549.1:n.*51G>A