Canonical Allele Identifier: CA2388025731

Gene: CLDN14 CLDN14-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.36479752T= , CM000683.2:g.36479752T=	GRCh38
NC_000021.8:g.37852050T= , CM000683.1:g.37852050T=	GRCh37
NC_000021.7:g.36773920T=	NCBI36
NG_011777.1:g.101818A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399135.6:c.-339A= (CLDN14) MANE Select	ENSP00000382087.1:n.-339A=
ENST00000342108.2:c.-81-17976A= (CLDN14)	ENSP00000339292.2:n.-81-17976A=
ENST00000399135.5:c.-339A= (CLDN14)	ENSP00000382087.1:n.-339A=
ENST00000399136.5:c.-81-17976A= (CLDN14)	ENSP00000382088.1:n.-81-17976A=
ENST00000399137.5:c.-529A= (CLDN14)	ENSP00000382090.1:n.-529A=
NM_001146077.1:c.-81-17976A= (CLDN14)	NP_001139549.1:n.-81-17976A=
NM_001146078.2:c.-81-17976A= (CLDN14)	NP_001139550.1:n.-81-17976A=
NM_001146079.1:c.-339A= (CLDN14)	NP_001139551.1:n.-339A=
NM_144492.2:c.-529A= (CLDN14)	NP_652763.1:n.-529A=
XM_011529519.1:c.-81-17976A= (CLDN14)	XP_011527821.1:n.-81-17976A=
XR_937694.1:n.962-479T= (CLDN14-AS1)
XR_937695.1:n.469-479T= (CLDN14-AS1)
XR_937696.1:n.853-479T= (CLDN14-AS1)
XR_001755024.1:n.1022-479T= (CLDN14-AS1)
XR_001755025.1:n.469-479T= (CLDN14-AS1)
NM_001146079.2:c.-339A= (CLDN14) MANE Select	NP_001139551.1:n.-339A=
NM_001146078.3:c.-81-17976A= (CLDN14)	NP_001139550.1:n.-81-17976A=
NM_144492.3:c.-529A= (CLDN14)	NP_652763.1:n.-529A=
NM_001146077.2:c.-81-17976A= (CLDN14)	NP_001139549.1:n.-81-17976A=