Canonical Allele Identifier: CA355492228

Gene: SLC7A14 CLDN11 SLC7A14-AS1

Linked Data

• gnomAD v4: 3-170483517-G-T
• MyVariant Identifiers: chr3:g.170201306G>T (hg19) ; chr3:g.170483517G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.170483517G>T , CM000665.2:g.170483517G>T	GRCh38
NC_000003.11:g.170201306G>T , CM000665.1:g.170201306G>T	GRCh37
NC_000003.10:g.171684000G>T	NCBI36
NG_034121.1:g.107558C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231706.6:c.912C>A (SLC7A14) MANE Select	ENSP00000231706.4:p.Ser304Arg
ENST00000231706.5:c.912C>A (SLC7A14)	ENSP00000231706.4:p.Ser304Arg
ENST00000471373.5:n.373-19294G>T (CLDN11)
ENST00000480067.1:n.218+6644G>T (CLDN11)
ENST00000486975.1:c.391+60190G>T (CLDN11)	ENSP00000417434.1:n.391+60190G>T
NM_020949.2:c.912C>A (SLC7A14)	NP_066000.2:p.Ser304Arg
XM_011513058.1:c.-16C>A (SLC7A14)	XP_011511360.1:n.-16C>A
NR_135555.1:n.215+6644G>T (SLC7A14-AS1)
NR_135556.1:n.215+6644G>T (SLC7A14-AS1)
NR_135557.1:n.221+6644G>T (SLC7A14-AS1)
NM_020949.3:c.912C>A (SLC7A14) MANE Select	NP_066000.2:p.Ser304Arg