Canonical Allele Identifier: CA1419943267

Gene: SLC7A14 CLDN11 SLC7A14-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.170483747_170483751delinsACTCT , CM000665.2:g.170483747_170483751delinsACTCT	GRCh38
NC_000003.11:g.170201536_170201540delinsACTCT , CM000665.1:g.170201536_170201540delinsACTCT	GRCh37
NC_000003.10:g.171684230_171684234delinsACTCT	NCBI36
NG_034121.1:g.107324_107328delinsAGAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231706.6:c.907-229_907-225delinsAGAGT (SLC7A14) MANE Select	ENSP00000231706.4:n.907-229_907-225delinsAGAGT
ENST00000231706.5:c.907-229_907-225delinsAGAGT (SLC7A14)	ENSP00000231706.4:n.907-229_907-225delinsAGAGT
ENST00000471373.5:n.373-19064_373-19060delinsACTCT (CLDN11)
ENST00000480067.1:n.218+6874_218+6878delinsACTCT (CLDN11)
ENST00000486975.1:c.391+60420_391+60424delinsACTCT (CLDN11)	ENSP00000417434.1:n.391+60420_391+60424delinsACTCT
NM_020949.2:c.907-229_907-225delinsAGAGT (SLC7A14)	NP_066000.2:n.907-229_907-225delinsAGAGT
XM_011513058.1:c.-21-229_-21-225delinsAGAGT (SLC7A14)	XP_011511360.1:n.-21-229_-21-225delinsAGAGT
NR_135555.1:n.215+6874_215+6878delinsACTCT (SLC7A14-AS1)
NR_135556.1:n.215+6874_215+6878delinsACTCT (SLC7A14-AS1)
NR_135557.1:n.221+6874_221+6878delinsACTCT (SLC7A14-AS1)
NM_020949.3:c.907-229_907-225delinsAGAGT (SLC7A14) MANE Select	NP_066000.2:n.907-229_907-225delinsAGAGT