Canonical Allele Identifier: CA87712711
Gene: SLC7A14 HGNC NCBI
CLDN11 HGNC NCBI
SLC7A14-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1016092908
MyVariant Identifiers: chr3:g.170201295G>T (hg19) chr3:g.170483506G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.170483506G>T , CM000665.2:g.170483506G>T GRCh38
NC_000003.11:g.170201295G>T , CM000665.1:g.170201295G>T GRCh37
NC_000003.10:g.171683989G>T NCBI36
NG_034121.1:g.107569C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000231706.6:c.923C>A (SLC7A14) MANE Select ENSP00000231706.4:p.Thr308Asn
ENST00000231706.5:c.923C>A (SLC7A14) ENSP00000231706.4:p.Thr308Asn
ENST00000471373.5:n.373-19305G>T (CLDN11)
ENST00000480067.1:n.218+6633G>T (CLDN11)
ENST00000486975.1:c.391+60179G>T (CLDN11) ENSP00000417434.1:n.391+60179G>T
NM_020949.2:c.923C>A (SLC7A14) NP_066000.2:p.Thr308Asn
XM_011513058.1:c.-5C>A (SLC7A14) XP_011511360.1:n.-5C>A
NR_135555.1:n.215+6633G>T (SLC7A14-AS1)
NR_135556.1:n.215+6633G>T (SLC7A14-AS1)
NR_135557.1:n.221+6633G>T (SLC7A14-AS1)
NM_020949.3:c.923C>A (SLC7A14) MANE Select NP_066000.2:p.Thr308Asn
Search 100 bp 5'
Search 100 bp 3'