Canonical Allele Identifier: CA2759362280

Gene: SLC7A14 CLDN11 SLC7A14-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.170483703_170483707del , CM000665.2:g.170483703_170483707del	GRCh38
NC_000003.11:g.170201492_170201496del , CM000665.1:g.170201492_170201496del	GRCh37
NC_000003.10:g.171684186_171684190del	NCBI36
NG_034121.1:g.107368_107372del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231706.6:c.907-185_907-181del (SLC7A14) MANE Select	ENSP00000231706.4:n.907-185_907-181del
ENST00000231706.5:c.907-185_907-181del (SLC7A14)	ENSP00000231706.4:n.907-185_907-181del
ENST00000471373.5:n.373-19108_373-19104del (CLDN11)
ENST00000480067.1:n.218+6830_218+6834del (CLDN11)
ENST00000486975.1:c.391+60376_391+60380del (CLDN11)	ENSP00000417434.1:n.391+60376_391+60380del
NM_020949.2:c.907-185_907-181del (SLC7A14)	NP_066000.2:n.907-185_907-181del
XM_011513058.1:c.-21-185_-21-181del (SLC7A14)	XP_011511360.1:n.-21-185_-21-181del
NR_135555.1:n.215+6830_215+6834del (SLC7A14-AS1)
NR_135556.1:n.215+6830_215+6834del (SLC7A14-AS1)
NR_135557.1:n.221+6830_221+6834del (SLC7A14-AS1)
NM_020949.3:c.907-185_907-181del (SLC7A14) MANE Select	NP_066000.2:n.907-185_907-181del