Canonical Allele Identifier: CA355492177

Gene: SLC7A14 CLDN11 SLC7A14-AS1

Linked Data

• MyVariant Identifiers: chr3:g.170201281A>G (hg19) ; chr3:g.170483492A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.170483492A>G , CM000665.2:g.170483492A>G	GRCh38
NC_000003.11:g.170201281A>G , CM000665.1:g.170201281A>G	GRCh37
NC_000003.10:g.171683975A>G	NCBI36
NG_034121.1:g.107583T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231706.6:c.937T>C (SLC7A14) MANE Select	ENSP00000231706.4:p.Tyr313His
ENST00000231706.5:c.937T>C (SLC7A14)	ENSP00000231706.4:p.Tyr313His
ENST00000471373.5:n.373-19319A>G (CLDN11)
ENST00000480067.1:n.218+6619A>G (CLDN11)
ENST00000486975.1:c.391+60165A>G (CLDN11)	ENSP00000417434.1:n.391+60165A>G
NM_020949.2:c.937T>C (SLC7A14)	NP_066000.2:p.Tyr313His
XM_011513058.1:c.10T>C (SLC7A14)	XP_011511360.1:p.Tyr4His
NR_135555.1:n.215+6619A>G (SLC7A14-AS1)
NR_135556.1:n.215+6619A>G (SLC7A14-AS1)
NR_135557.1:n.221+6619A>G (SLC7A14-AS1)
NM_020949.3:c.937T>C (SLC7A14) MANE Select	NP_066000.2:p.Tyr313His