Canonical Allele Identifier: CA355491908
Gene: SLC7A14 HGNC NCBI
CLDN11 HGNC NCBI
SLC7A14-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.170201149T>C (hg19) chr3:g.170483360T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.170483360T>C , CM000665.2:g.170483360T>C GRCh38
NC_000003.11:g.170201149T>C , CM000665.1:g.170201149T>C GRCh37
NC_000003.10:g.171683843T>C NCBI36
NG_034121.1:g.107715A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000231706.6:c.1069A>G (SLC7A14) MANE Select ENSP00000231706.4:p.Met357Val
ENST00000231706.5:c.1069A>G (SLC7A14) ENSP00000231706.4:p.Met357Val
ENST00000471373.5:n.373-19451T>C (CLDN11)
ENST00000480067.1:n.218+6487T>C (CLDN11)
ENST00000486975.1:c.391+60033T>C (CLDN11) ENSP00000417434.1:n.391+60033T>C
NM_020949.2:c.1069A>G (SLC7A14) NP_066000.2:p.Met357Val
XM_011513058.1:c.142A>G (SLC7A14) XP_011511360.1:p.Met48Val
NR_135555.1:n.215+6487T>C (SLC7A14-AS1)
NR_135556.1:n.215+6487T>C (SLC7A14-AS1)
NR_135557.1:n.221+6487T>C (SLC7A14-AS1)
NM_020949.3:c.1069A>G (SLC7A14) MANE Select NP_066000.2:p.Met357Val
Search 100 bp 5'
Search 100 bp 3'