Canonical Allele Identifier: CA2668515359
Gene: SLC7A14 HGNC NCBI
CLDN11 HGNC NCBI
SLC7A14-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.170483250_170483258del , CM000665.2:g.170483250_170483258del GRCh38
NC_000003.11:g.170201039_170201047del , CM000665.1:g.170201039_170201047del GRCh37
NC_000003.10:g.171683733_171683741del NCBI36
NG_034121.1:g.107817_107825del

Transcript Alleles

HGVS Amino-acid Change
ENST00000231706.6:c.1115+56_1115+64del (SLC7A14) MANE Select ENSP00000231706.4:n.1115+56_1115+64del
ENST00000231706.5:c.1115+56_1115+64del (SLC7A14) ENSP00000231706.4:n.1115+56_1115+64del
ENST00000471373.5:n.373-19561_373-19553del (CLDN11)
ENST00000480067.1:n.218+6377_218+6385del (CLDN11)
ENST00000486975.1:c.391+59923_391+59931del (CLDN11) ENSP00000417434.1:n.391+59923_391+59931del
NM_020949.2:c.1115+56_1115+64del (SLC7A14) NP_066000.2:n.1115+56_1115+64del
XM_011513058.1:c.188+56_188+64del (SLC7A14) XP_011511360.1:n.188+56_188+64del
NR_135555.1:n.215+6377_215+6385del (SLC7A14-AS1)
NR_135556.1:n.215+6377_215+6385del (SLC7A14-AS1)
NR_135557.1:n.221+6377_221+6385del (SLC7A14-AS1)
NM_020949.3:c.1115+56_1115+64del (SLC7A14) MANE Select NP_066000.2:n.1115+56_1115+64del