Canonical Allele Identifier: CA1419943197

Gene: SLC7A14 CLDN11 SLC7A14-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.170483670_170483671delinsTG , CM000665.2:g.170483670_170483671delinsTG	GRCh38
NC_000003.11:g.170201459_170201460delinsTG , CM000665.1:g.170201459_170201460delinsTG	GRCh37
NC_000003.10:g.171684153_171684154delinsTG	NCBI36
NG_034121.1:g.107404_107405delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231706.6:c.907-149_907-148delinsCA (SLC7A14) MANE Select	ENSP00000231706.4:n.907-149_907-148delinsCA
ENST00000231706.5:c.907-149_907-148delinsCA (SLC7A14)	ENSP00000231706.4:n.907-149_907-148delinsCA
ENST00000471373.5:n.373-19141_373-19140delinsTG (CLDN11)
ENST00000480067.1:n.218+6797_218+6798delinsTG (CLDN11)
ENST00000486975.1:c.391+60343_391+60344delinsTG (CLDN11)	ENSP00000417434.1:n.391+60343_391+60344delinsTG
NM_020949.2:c.907-149_907-148delinsCA (SLC7A14)	NP_066000.2:n.907-149_907-148delinsCA
XM_011513058.1:c.-21-149_-21-148delinsCA (SLC7A14)	XP_011511360.1:n.-21-149_-21-148delinsCA
NR_135555.1:n.215+6797_215+6798delinsTG (SLC7A14-AS1)
NR_135556.1:n.215+6797_215+6798delinsTG (SLC7A14-AS1)
NR_135557.1:n.221+6797_221+6798delinsTG (SLC7A14-AS1)
NM_020949.3:c.907-149_907-148delinsCA (SLC7A14) MANE Select	NP_066000.2:n.907-149_907-148delinsCA