Canonical Allele Identifier: CA10019341

Gene: CLDN14 CLDN14-AS1

Linked Data

• dbSNP Id: rs142205038
• ExAC: 21:37833888 C / A
• gnomAD v2: 21-37833888-C-A
• gnomAD v3: 21-36461590-C-A
• gnomAD v4: 21-36461590-C-A
• MyVariant Identifiers: chr21:g.37833888C>A (hg19) ; chr21:g.36461590C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.36461590C>A , CM000683.2:g.36461590C>A	GRCh38
NC_000021.8:g.37833888C>A , CM000683.1:g.37833888C>A	GRCh37
NC_000021.7:g.36755758C>A	NCBI36
NG_011777.1:g.119980G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000399135.6:c.106G>T (CLDN14) MANE Select	ENSP00000382087.1:p.Val36Leu
ENST00000342108.2:c.106G>T (CLDN14)	ENSP00000339292.2:p.Val36Leu
ENST00000399135.5:c.106G>T (CLDN14)	ENSP00000382087.1:p.Val36Leu
ENST00000399136.5:c.106G>T (CLDN14)	ENSP00000382088.1:p.Val36Leu
ENST00000399137.5:c.106G>T (CLDN14)	ENSP00000382090.1:p.Val36Leu
ENST00000399139.5:c.106G>T (CLDN14)	ENSP00000382092.1:p.Val36Leu
NM_001146077.1:c.106G>T (CLDN14)	NP_001139549.1:p.Val36Leu
NM_001146078.2:c.106G>T (CLDN14)	NP_001139550.1:p.Val36Leu
NM_001146079.1:c.106G>T (CLDN14)	NP_001139551.1:p.Val36Leu
NM_012130.3:c.106G>T (CLDN14)	NP_036262.1:p.Val36Leu
NM_144492.2:c.106G>T (CLDN14)	NP_652763.1:p.Val36Leu
XM_011529519.1:c.106G>T (CLDN14)	XP_011527821.1:p.Val36Leu
XR_937694.1:n.468+15583C>A (CLDN14-AS1)
XR_937695.1:n.468+15583C>A (CLDN14-AS1)
XR_937696.1:n.468+15583C>A (CLDN14-AS1)
XR_001755025.1:n.468+15583C>A (CLDN14-AS1)
NM_001146079.2:c.106G>T (CLDN14) MANE Select	NP_001139551.1:p.Val36Leu
NM_001146078.3:c.106G>T (CLDN14)	NP_001139550.1:p.Val36Leu
NM_012130.4:c.106G>T (CLDN14)	NP_036262.1:p.Val36Leu
NM_144492.3:c.106G>T (CLDN14)	NP_652763.1:p.Val36Leu
NM_001146077.2:c.106G>T (CLDN14)	NP_001139549.1:p.Val36Leu