Canonical Allele Identifier: CA2388017587

Gene: CLDN14 CLDN14-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.36461208G= , CM000683.2:g.36461208G=	GRCh38
NC_000021.8:g.37833506G= , CM000683.1:g.37833506G=	GRCh37
NC_000021.7:g.36755376G=	NCBI36
NG_011777.1:g.120362C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001146079.2:c.488C= (CLDN14) MANE Select	NP_001139551.1:p.Ala163=
ENST00000399135.6:c.488C= (CLDN14) MANE Select	ENSP00000382087.1:p.Ala163=
NM_001146077.1:c.488C= (CLDN14)	NP_001139549.1:p.Ala163=
NM_001146077.2:c.488C= (CLDN14)	NP_001139549.1:p.Ala163=
NM_001146078.2:c.488C= (CLDN14)	NP_001139550.1:p.Ala163=
NM_001146078.3:c.488C= (CLDN14)	NP_001139550.1:p.Ala163=
NM_001146079.1:c.488C= (CLDN14)	NP_001139551.1:p.Ala163=
NM_012130.3:c.488C= (CLDN14)	NP_036262.1:p.Ala163=
NM_012130.4:c.488C= (CLDN14)	NP_036262.1:p.Ala163=
NM_144492.2:c.488C= (CLDN14)	NP_652763.1:p.Ala163=
NM_144492.3:c.488C= (CLDN14)	NP_652763.1:p.Ala163=
ENST00000342108.2:c.488C= (CLDN14)	ENSP00000339292.2:p.Ala163=
ENST00000399135.5:c.488C= (CLDN14)	ENSP00000382087.1:p.Ala163=
ENST00000399136.5:c.488C= (CLDN14)	ENSP00000382088.1:p.Ala163=
ENST00000399137.5:c.488C= (CLDN14)	ENSP00000382090.1:p.Ala163=
ENST00000399139.5:c.488C= (CLDN14)	ENSP00000382092.1:p.Ala163=
XM_011529519.1:c.488C= (CLDN14)	XP_011527821.1:p.Ala163=
XR_001755025.1:n.468+15201G= (CLDN14-AS1)
XR_937694.1:n.468+15201G= (CLDN14-AS1)
XR_937695.1:n.468+15201G= (CLDN14-AS1)
XR_937696.1:n.468+15201G= (CLDN14-AS1)