Canonical Allele Identifier: CA1419943013

Gene: SLC7A14 CLDN11 SLC7A14-AS1

Linked Data

• dbSNP Id: rs1711913760
• gnomAD v4: 3-170483467-G-GGGGATTCC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.170483469_170483476dup , CM000665.2:g.170483469_170483476dup	GRCh38
NC_000003.11:g.170201258_170201265dup , CM000665.1:g.170201258_170201265dup	GRCh37
NC_000003.10:g.171683952_171683959dup	NCBI36
NG_034121.1:g.107600_107607dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231706.6:c.954_961dup (SLC7A14) MANE Select	ENSP00000231706.4:p.Pro321ArgfsTer20
ENST00000231706.5:c.954_961dup (SLC7A14)	ENSP00000231706.4:p.Pro321ArgfsTer20
ENST00000471373.5:n.373-19342_373-19335dup (CLDN11)
ENST00000480067.1:n.218+6596_218+6603dup (CLDN11)
ENST00000486975.1:c.391+60142_391+60149dup (CLDN11)	ENSP00000417434.1:n.391+60142_391+60149dup
NM_020949.2:c.954_961dup (SLC7A14)	NP_066000.2:p.Pro321ArgfsTer20
XM_011513058.1:c.27_34dup (SLC7A14)	XP_011511360.1:p.Pro12ArgfsTer20
NR_135555.1:n.215+6596_215+6603dup (SLC7A14-AS1)
NR_135556.1:n.215+6596_215+6603dup (SLC7A14-AS1)
NR_135557.1:n.221+6596_221+6603dup (SLC7A14-AS1)
NM_020949.3:c.954_961dup (SLC7A14) MANE Select	NP_066000.2:p.Pro321ArgfsTer20