Canonical Allele Identifier: CA638055534

Gene: CLDN14 CLDN14-AS1

Linked Data

• dbSNP Id: rs1568839836
• gnomAD v2: 21-37834022-GC-G
• gnomAD v3: 21-36461724-GC-G
• gnomAD v4: 21-36461724-GC-G
• MyVariant Identifiers: chr21:g.37834023del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.36461725del , CM000683.2:g.36461725del	GRCh38
NC_000021.8:g.37834023del , CM000683.1:g.37834023del	GRCh37
NC_000021.7:g.36755893del	NCBI36
NG_011777.1:g.119845del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399135.6:c.-30del (CLDN14) MANE Select	ENSP00000382087.1:n.-30del
ENST00000342108.2:c.-30del (CLDN14)	ENSP00000339292.2:n.-30del
ENST00000399135.5:c.-30del (CLDN14)	ENSP00000382087.1:n.-30del
ENST00000399136.5:c.-30del (CLDN14)	ENSP00000382088.1:n.-30del
ENST00000399137.5:c.-30del (CLDN14)	ENSP00000382090.1:n.-30del
ENST00000399139.5:c.-30del (CLDN14)	ENSP00000382092.1:n.-30del
NM_001146077.1:c.-30del (CLDN14)	NP_001139549.1:n.-30del
NM_001146078.2:c.-30del (CLDN14)	NP_001139550.1:n.-30del
NM_001146079.1:c.-30del (CLDN14)	NP_001139551.1:n.-30del
NM_012130.3:c.-30del (CLDN14)	NP_036262.1:n.-30del
NM_144492.2:c.-30del (CLDN14)	NP_652763.1:n.-30del
XM_011529519.1:c.-30del (CLDN14)	XP_011527821.1:n.-30del
XR_937694.1:n.468+15718del (CLDN14-AS1)
XR_937695.1:n.468+15718del (CLDN14-AS1)
XR_937696.1:n.468+15718del (CLDN14-AS1)
XR_001755025.1:n.468+15718del (CLDN14-AS1)
NM_001146079.2:c.-30del (CLDN14) MANE Select	NP_001139551.1:n.-30del
NM_001146078.3:c.-30del (CLDN14)	NP_001139550.1:n.-30del
NM_012130.4:c.-30del (CLDN14)	NP_036262.1:n.-30del
NM_144492.3:c.-30del (CLDN14)	NP_652763.1:n.-30del
NM_001146077.2:c.-30del (CLDN14)	NP_001139549.1:n.-30del