Canonical Allele Identifier: CA2759362207

Gene: SLC7A14 CLDN11 SLC7A14-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.170483240_170483243del , CM000665.2:g.170483240_170483243del	GRCh38
NC_000003.11:g.170201029_170201032del , CM000665.1:g.170201029_170201032del	GRCh37
NC_000003.10:g.171683723_171683726del	NCBI36
NG_034121.1:g.107833_107836del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231706.6:c.1115+72_1115+75del (SLC7A14) MANE Select	ENSP00000231706.4:n.1115+72_1115+75del
ENST00000231706.5:c.1115+72_1115+75del (SLC7A14)	ENSP00000231706.4:n.1115+72_1115+75del
ENST00000471373.5:n.373-19571_373-19568del (CLDN11)
ENST00000480067.1:n.218+6367_218+6370del (CLDN11)
ENST00000486975.1:c.391+59913_391+59916del (CLDN11)	ENSP00000417434.1:n.391+59913_391+59916del
NM_020949.2:c.1115+72_1115+75del (SLC7A14)	NP_066000.2:n.1115+72_1115+75del
XM_011513058.1:c.188+72_188+75del (SLC7A14)	XP_011511360.1:n.188+72_188+75del
NR_135555.1:n.215+6367_215+6370del (SLC7A14-AS1)
NR_135556.1:n.215+6367_215+6370del (SLC7A14-AS1)
NR_135557.1:n.221+6367_221+6370del (SLC7A14-AS1)
NM_020949.3:c.1115+72_1115+75del (SLC7A14) MANE Select	NP_066000.2:n.1115+72_1115+75del