Canonical Allele Identifier: CA355492217

Gene: SLC7A14 CLDN11 SLC7A14-AS1

Linked Data

• MyVariant Identifiers: chr3:g.170201301A>G (hg19) ; chr3:g.170483512A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.170483512A>G , CM000665.2:g.170483512A>G	GRCh38
NC_000003.11:g.170201301A>G , CM000665.1:g.170201301A>G	GRCh37
NC_000003.10:g.171683995A>G	NCBI36
NG_034121.1:g.107563T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231706.6:c.917T>C (SLC7A14) MANE Select	ENSP00000231706.4:p.Ile306Thr
ENST00000231706.5:c.917T>C (SLC7A14)	ENSP00000231706.4:p.Ile306Thr
ENST00000471373.5:n.373-19299A>G (CLDN11)
ENST00000480067.1:n.218+6639A>G (CLDN11)
ENST00000486975.1:c.391+60185A>G (CLDN11)	ENSP00000417434.1:n.391+60185A>G
NM_020949.2:c.917T>C (SLC7A14)	NP_066000.2:p.Ile306Thr
XM_011513058.1:c.-11T>C (SLC7A14)	XP_011511360.1:n.-11T>C
NR_135555.1:n.215+6639A>G (SLC7A14-AS1)
NR_135556.1:n.215+6639A>G (SLC7A14-AS1)
NR_135557.1:n.221+6639A>G (SLC7A14-AS1)
NM_020949.3:c.917T>C (SLC7A14) MANE Select	NP_066000.2:p.Ile306Thr