Canonical Allele Identifier: CA1419943030

Gene: SLC7A14 CLDN11 SLC7A14-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.170483476G= , CM000665.2:g.170483476G=	GRCh38
NC_000003.11:g.170201265G= , CM000665.1:g.170201265G=	GRCh37
NC_000003.10:g.171683959G=	NCBI36
NG_034121.1:g.107599C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231706.6:c.953C= (SLC7A14) MANE Select	ENSP00000231706.4:p.Thr318=
ENST00000231706.5:c.953C= (SLC7A14)	ENSP00000231706.4:p.Thr318=
ENST00000471373.5:n.373-19335G= (CLDN11)
ENST00000480067.1:n.218+6603G= (CLDN11)
ENST00000486975.1:c.391+60149G= (CLDN11)	ENSP00000417434.1:n.391+60149G=
NM_020949.2:c.953C= (SLC7A14)	NP_066000.2:p.Thr318=
XM_011513058.1:c.26C= (SLC7A14)	XP_011511360.1:p.Thr9=
NR_135555.1:n.215+6603G= (SLC7A14-AS1)
NR_135556.1:n.215+6603G= (SLC7A14-AS1)
NR_135557.1:n.221+6603G= (SLC7A14-AS1)
NM_020949.3:c.953C= (SLC7A14) MANE Select	NP_066000.2:p.Thr318=