Canonical Allele Identifier: CA355492013

Gene: SLC7A14 CLDN11 SLC7A14-AS1

Linked Data

• gnomAD v4: 3-170483417-C-T
• MyVariant Identifiers: chr3:g.170201206C>T (hg19) ; chr3:g.170483417C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.170483417C>T , CM000665.2:g.170483417C>T	GRCh38
NC_000003.11:g.170201206C>T , CM000665.1:g.170201206C>T	GRCh37
NC_000003.10:g.171683900C>T	NCBI36
NG_034121.1:g.107658G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231706.6:c.1012G>A (SLC7A14) MANE Select	ENSP00000231706.4:p.Val338Met
ENST00000231706.5:c.1012G>A (SLC7A14)	ENSP00000231706.4:p.Val338Met
ENST00000471373.5:n.373-19394C>T (CLDN11)
ENST00000480067.1:n.218+6544C>T (CLDN11)
ENST00000486975.1:c.391+60090C>T (CLDN11)	ENSP00000417434.1:n.391+60090C>T
NM_020949.2:c.1012G>A (SLC7A14)	NP_066000.2:p.Val338Met
XM_011513058.1:c.85G>A (SLC7A14)	XP_011511360.1:p.Val29Met
NR_135555.1:n.215+6544C>T (SLC7A14-AS1)
NR_135556.1:n.215+6544C>T (SLC7A14-AS1)
NR_135557.1:n.221+6544C>T (SLC7A14-AS1)
NM_020949.3:c.1012G>A (SLC7A14) MANE Select	NP_066000.2:p.Val338Met