Canonical Allele Identifier: CA436773935

Gene: SLC7A14 CLDN11 SLC7A14-AS1

Linked Data

• dbSNP Id: rs1711915552
• MyVariant Identifiers: chr3:g.170201291C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.170483502C>G , CM000665.2:g.170483502C>G	GRCh38
NC_000003.11:g.170201291C>G , CM000665.1:g.170201291C>G	GRCh37
NC_000003.10:g.171683985C>G	NCBI36
NG_034121.1:g.107573G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231706.6:c.927G>C (SLC7A14) MANE Select	ENSP00000231706.4:p.Leu309=
ENST00000231706.5:c.927G>C (SLC7A14)	ENSP00000231706.4:p.Leu309=
ENST00000471373.5:n.373-19309C>G (CLDN11)
ENST00000480067.1:n.218+6629C>G (CLDN11)
ENST00000486975.1:c.391+60175C>G (CLDN11)	ENSP00000417434.1:n.391+60175C>G
NM_020949.2:c.927G>C (SLC7A14)	NP_066000.2:p.Leu309=
XM_011513058.1:c.-1G>C (SLC7A14)	XP_011511360.1:n.-1G>C
NR_135555.1:n.215+6629C>G (SLC7A14-AS1)
NR_135556.1:n.215+6629C>G (SLC7A14-AS1)
NR_135557.1:n.221+6629C>G (SLC7A14-AS1)
NM_020949.3:c.927G>C (SLC7A14) MANE Select	NP_066000.2:p.Leu309=