Canonical Allele Identifier: CA1419943303
Gene: SLC7A14 HGNC NCBI
CLDN11 HGNC NCBI
SLC7A14-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.170483802_170483803delinsGC , CM000665.2:g.170483802_170483803delinsGC GRCh38
NC_000003.11:g.170201591_170201592delinsGC , CM000665.1:g.170201591_170201592delinsGC GRCh37
NC_000003.10:g.171684285_171684286delinsGC NCBI36
NG_034121.1:g.107272_107273delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000231706.6:c.907-281_907-280delinsGC (SLC7A14) MANE Select ENSP00000231706.4:n.907-281_907-280delinsGC
ENST00000231706.5:c.907-281_907-280delinsGC (SLC7A14) ENSP00000231706.4:n.907-281_907-280delinsGC
ENST00000471373.5:n.373-19009_373-19008delinsGC (CLDN11)
ENST00000480067.1:n.218+6929_218+6930delinsGC (CLDN11)
ENST00000486975.1:c.391+60475_391+60476delinsGC (CLDN11) ENSP00000417434.1:n.391+60475_391+60476delinsGC
NM_020949.2:c.907-281_907-280delinsGC (SLC7A14) NP_066000.2:n.907-281_907-280delinsGC
XM_011513058.1:c.-21-281_-21-280delinsGC (SLC7A14) XP_011511360.1:n.-21-281_-21-280delinsGC
NR_135555.1:n.215+6929_215+6930delinsGC (SLC7A14-AS1)
NR_135556.1:n.215+6929_215+6930delinsGC (SLC7A14-AS1)
NR_135557.1:n.221+6929_221+6930delinsGC (SLC7A14-AS1)
NM_020949.3:c.907-281_907-280delinsGC (SLC7A14) MANE Select NP_066000.2:n.907-281_907-280delinsGC