Canonical Allele Identifier: CA409881448

Gene: CLDN14 CLDN14-AS1

Linked Data

• gnomAD v4: 21-36461218-T-C
• MyVariant Identifiers: chr21:g.37833516T>C (hg19) ; chr21:g.36461218T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.36461218T>C , CM000683.2:g.36461218T>C	GRCh38
NC_000021.8:g.37833516T>C , CM000683.1:g.37833516T>C	GRCh37
NC_000021.7:g.36755386T>C	NCBI36
NG_011777.1:g.120352A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399135.6:c.478A>G (CLDN14) MANE Select	ENSP00000382087.1:p.Ile160Val
ENST00000342108.2:c.478A>G (CLDN14)	ENSP00000339292.2:p.Ile160Val
ENST00000399135.5:c.478A>G (CLDN14)	ENSP00000382087.1:p.Ile160Val
ENST00000399136.5:c.478A>G (CLDN14)	ENSP00000382088.1:p.Ile160Val
ENST00000399137.5:c.478A>G (CLDN14)	ENSP00000382090.1:p.Ile160Val
ENST00000399139.5:c.478A>G (CLDN14)	ENSP00000382092.1:p.Ile160Val
NM_001146077.1:c.478A>G (CLDN14)	NP_001139549.1:p.Ile160Val
NM_001146078.2:c.478A>G (CLDN14)	NP_001139550.1:p.Ile160Val
NM_001146079.1:c.478A>G (CLDN14)	NP_001139551.1:p.Ile160Val
NM_012130.3:c.478A>G (CLDN14)	NP_036262.1:p.Ile160Val
NM_144492.2:c.478A>G (CLDN14)	NP_652763.1:p.Ile160Val
XM_011529519.1:c.478A>G (CLDN14)	XP_011527821.1:p.Ile160Val
XR_937694.1:n.468+15211T>C (CLDN14-AS1)
XR_937695.1:n.468+15211T>C (CLDN14-AS1)
XR_937696.1:n.468+15211T>C (CLDN14-AS1)
XR_001755025.1:n.468+15211T>C (CLDN14-AS1)
NM_001146079.2:c.478A>G (CLDN14) MANE Select	NP_001139551.1:p.Ile160Val
NM_001146078.3:c.478A>G (CLDN14)	NP_001139550.1:p.Ile160Val
NM_012130.4:c.478A>G (CLDN14)	NP_036262.1:p.Ile160Val
NM_144492.3:c.478A>G (CLDN14)	NP_652763.1:p.Ile160Val
NM_001146077.2:c.478A>G (CLDN14)	NP_001139549.1:p.Ile160Val