Canonical Allele Identifier: CA1419943055

Gene: SLC7A14 CLDN11 SLC7A14-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.170483495G= , CM000665.2:g.170483495G=	GRCh38
NC_000003.11:g.170201284G= , CM000665.1:g.170201284G=	GRCh37
NC_000003.10:g.171683978G=	NCBI36
NG_034121.1:g.107580C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231706.6:c.934C= (SLC7A14) MANE Select	ENSP00000231706.4:p.Pro312=
ENST00000231706.5:c.934C= (SLC7A14)	ENSP00000231706.4:p.Pro312=
ENST00000471373.5:n.373-19316G= (CLDN11)
ENST00000480067.1:n.218+6622G= (CLDN11)
ENST00000486975.1:c.391+60168G= (CLDN11)	ENSP00000417434.1:n.391+60168G=
NM_020949.2:c.934C= (SLC7A14)	NP_066000.2:p.Pro312=
XM_011513058.1:c.7C= (SLC7A14)	XP_011511360.1:p.Pro3=
NR_135555.1:n.215+6622G= (SLC7A14-AS1)
NR_135556.1:n.215+6622G= (SLC7A14-AS1)
NR_135557.1:n.221+6622G= (SLC7A14-AS1)
NM_020949.3:c.934C= (SLC7A14) MANE Select	NP_066000.2:p.Pro312=