Canonical Allele Identifier: CA2668515494

Gene: SLC7A14 CLDN11 SLC7A14-AS1

Linked Data

• gnomAD v4: 3-170483466-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.170483470del , CM000665.2:g.170483470del	GRCh38
NC_000003.11:g.170201259del , CM000665.1:g.170201259del	GRCh37
NC_000003.10:g.171683953del	NCBI36
NG_034121.1:g.107608del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231706.6:c.962del (SLC7A14) MANE Select	ENSP00000231706.4:p.Pro321HisfsTer17
ENST00000231706.5:c.962del (SLC7A14)	ENSP00000231706.4:p.Pro321HisfsTer17
ENST00000471373.5:n.373-19341del (CLDN11)
ENST00000480067.1:n.218+6597del (CLDN11)
ENST00000486975.1:c.391+60143del (CLDN11)	ENSP00000417434.1:n.391+60143del
NM_020949.2:c.962del (SLC7A14)	NP_066000.2:p.Pro321HisfsTer17
XM_011513058.1:c.35del (SLC7A14)	XP_011511360.1:p.Pro12HisfsTer17
NR_135555.1:n.215+6597del (SLC7A14-AS1)
NR_135556.1:n.215+6597del (SLC7A14-AS1)
NR_135557.1:n.221+6597del (SLC7A14-AS1)
NM_020949.3:c.962del (SLC7A14) MANE Select	NP_066000.2:p.Pro321HisfsTer17