Canonical Allele Identifier: CA2704575463
Gene: SLC7A14 HGNC NCBI
CLDN11 HGNC NCBI
SLC7A14-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2108270695

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.170483820T>C , CM000665.2:g.170483820T>C GRCh38
NC_000003.11:g.170201609T>C , CM000665.1:g.170201609T>C GRCh37
NC_000003.10:g.171684303T>C NCBI36
NG_034121.1:g.107255A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000231706.6:c.907-298A>G (SLC7A14) MANE Select ENSP00000231706.4:n.907-298A>G
ENST00000231706.5:c.907-298A>G (SLC7A14) ENSP00000231706.4:n.907-298A>G
ENST00000471373.5:n.373-18991T>C (CLDN11)
ENST00000480067.1:n.218+6947T>C (CLDN11)
ENST00000486975.1:c.391+60493T>C (CLDN11) ENSP00000417434.1:n.391+60493T>C
NM_020949.2:c.907-298A>G (SLC7A14) NP_066000.2:n.907-298A>G
XM_011513058.1:c.-21-298A>G (SLC7A14) XP_011511360.1:n.-21-298A>G
NR_135555.1:n.215+6947T>C (SLC7A14-AS1)
NR_135556.1:n.215+6947T>C (SLC7A14-AS1)
NR_135557.1:n.221+6947T>C (SLC7A14-AS1)
NM_020949.3:c.907-298A>G (SLC7A14) MANE Select NP_066000.2:n.907-298A>G