Canonical Allele Identifier: CA355491872

Gene: SLC7A14 CLDN11 SLC7A14-AS1

Linked Data

• dbSNP Id: rs1711895510
• MyVariant Identifiers: chr3:g.170201133T>A (hg19) ; chr3:g.170483344T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.170483344T>A , CM000665.2:g.170483344T>A	GRCh38
NC_000003.11:g.170201133T>A , CM000665.1:g.170201133T>A	GRCh37
NC_000003.10:g.171683827T>A	NCBI36
NG_034121.1:g.107731A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231706.6:c.1085A>T (SLC7A14) MANE Select	ENSP00000231706.4:p.Tyr362Phe
ENST00000231706.5:c.1085A>T (SLC7A14)	ENSP00000231706.4:p.Tyr362Phe
ENST00000471373.5:n.373-19467T>A (CLDN11)
ENST00000480067.1:n.218+6471T>A (CLDN11)
ENST00000486975.1:c.391+60017T>A (CLDN11)	ENSP00000417434.1:n.391+60017T>A
NM_020949.2:c.1085A>T (SLC7A14)	NP_066000.2:p.Tyr362Phe
XM_011513058.1:c.158A>T (SLC7A14)	XP_011511360.1:p.Tyr53Phe
NR_135555.1:n.215+6471T>A (SLC7A14-AS1)
NR_135556.1:n.215+6471T>A (SLC7A14-AS1)
NR_135557.1:n.221+6471T>A (SLC7A14-AS1)
NM_020949.3:c.1085A>T (SLC7A14) MANE Select	NP_066000.2:p.Tyr362Phe