Canonical Allele Identifier: CA2759362263

Gene: SLC7A14 CLDN11 SLC7A14-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.170483646_170483647insACAA , CM000665.2:g.170483646_170483647insACAA	GRCh38
NC_000003.11:g.170201435_170201436insACAA , CM000665.1:g.170201435_170201436insACAA	GRCh37
NC_000003.10:g.171684129_171684130insACAA	NCBI36
NG_034121.1:g.107428_107429insTTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231706.6:c.907-125_907-124insTTGT (SLC7A14) MANE Select	ENSP00000231706.4:n.907-125_907-124insTTGT
ENST00000231706.5:c.907-125_907-124insTTGT (SLC7A14)	ENSP00000231706.4:n.907-125_907-124insTTGT
ENST00000471373.5:n.373-19165_373-19164insACAA (CLDN11)
ENST00000480067.1:n.218+6773_218+6774insACAA (CLDN11)
ENST00000486975.1:c.391+60319_391+60320insACAA (CLDN11)	ENSP00000417434.1:n.391+60319_391+60320insACAA
NM_020949.2:c.907-125_907-124insTTGT (SLC7A14)	NP_066000.2:n.907-125_907-124insTTGT
XM_011513058.1:c.-21-125_-21-124insTTGT (SLC7A14)	XP_011511360.1:n.-21-125_-21-124insTTGT
NR_135555.1:n.215+6773_215+6774insACAA (SLC7A14-AS1)
NR_135556.1:n.215+6773_215+6774insACAA (SLC7A14-AS1)
NR_135557.1:n.221+6773_221+6774insACAA (SLC7A14-AS1)
NM_020949.3:c.907-125_907-124insTTGT (SLC7A14) MANE Select	NP_066000.2:n.907-125_907-124insTTGT