Canonical Allele Identifier: CA355491933

Gene: SLC7A14 CLDN11 SLC7A14-AS1

Linked Data

• gnomAD v4: 3-170483374-C-A
• MyVariant Identifiers: chr3:g.170201163C>A (hg19) ; chr3:g.170483374C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.170483374C>A , CM000665.2:g.170483374C>A	GRCh38
NC_000003.11:g.170201163C>A , CM000665.1:g.170201163C>A	GRCh37
NC_000003.10:g.171683857C>A	NCBI36
NG_034121.1:g.107701G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231706.6:c.1055G>T (SLC7A14) MANE Select	ENSP00000231706.4:p.Gly352Val
ENST00000231706.5:c.1055G>T (SLC7A14)	ENSP00000231706.4:p.Gly352Val
ENST00000471373.5:n.373-19437C>A (CLDN11)
ENST00000480067.1:n.218+6501C>A (CLDN11)
ENST00000486975.1:c.391+60047C>A (CLDN11)	ENSP00000417434.1:n.391+60047C>A
NM_020949.2:c.1055G>T (SLC7A14)	NP_066000.2:p.Gly352Val
XM_011513058.1:c.128G>T (SLC7A14)	XP_011511360.1:p.Gly43Val
NR_135555.1:n.215+6501C>A (SLC7A14-AS1)
NR_135556.1:n.215+6501C>A (SLC7A14-AS1)
NR_135557.1:n.221+6501C>A (SLC7A14-AS1)
NM_020949.3:c.1055G>T (SLC7A14) MANE Select	NP_066000.2:p.Gly352Val