Canonical Allele Identifier: CA2759362259

Gene: SLC7A14 CLDN11 SLC7A14-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.170483638_170483639insACA , CM000665.2:g.170483638_170483639insACA	GRCh38
NC_000003.11:g.170201427_170201428insACA , CM000665.1:g.170201427_170201428insACA	GRCh37
NC_000003.10:g.171684121_171684122insACA	NCBI36
NG_034121.1:g.107436_107437insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231706.6:c.907-117_907-116insTGT (SLC7A14) MANE Select	ENSP00000231706.4:n.907-117_907-116insTGT
ENST00000231706.5:c.907-117_907-116insTGT (SLC7A14)	ENSP00000231706.4:n.907-117_907-116insTGT
ENST00000471373.5:n.373-19173_373-19172insACA (CLDN11)
ENST00000480067.1:n.218+6765_218+6766insACA (CLDN11)
ENST00000486975.1:c.391+60311_391+60312insACA (CLDN11)	ENSP00000417434.1:n.391+60311_391+60312insACA
NM_020949.2:c.907-117_907-116insTGT (SLC7A14)	NP_066000.2:n.907-117_907-116insTGT
XM_011513058.1:c.-21-117_-21-116insTGT (SLC7A14)	XP_011511360.1:n.-21-117_-21-116insTGT
NR_135555.1:n.215+6765_215+6766insACA (SLC7A14-AS1)
NR_135556.1:n.215+6765_215+6766insACA (SLC7A14-AS1)
NR_135557.1:n.221+6765_221+6766insACA (SLC7A14-AS1)
NM_020949.3:c.907-117_907-116insTGT (SLC7A14) MANE Select	NP_066000.2:n.907-117_907-116insTGT