Canonical Allele Identifier: CA1419943315
Gene: SLC7A14 HGNC NCBI
CLDN11 HGNC NCBI
SLC7A14-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.170483812_170483813delinsCA , CM000665.2:g.170483812_170483813delinsCA GRCh38
NC_000003.11:g.170201601_170201602delinsCA , CM000665.1:g.170201601_170201602delinsCA GRCh37
NC_000003.10:g.171684295_171684296delinsCA NCBI36
NG_034121.1:g.107262_107263delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000231706.6:c.907-291_907-290delinsTG (SLC7A14) MANE Select ENSP00000231706.4:n.907-291_907-290delinsTG
ENST00000231706.5:c.907-291_907-290delinsTG (SLC7A14) ENSP00000231706.4:n.907-291_907-290delinsTG
ENST00000471373.5:n.373-18999_373-18998delinsCA (CLDN11)
ENST00000480067.1:n.218+6939_218+6940delinsCA (CLDN11)
ENST00000486975.1:c.391+60485_391+60486delinsCA (CLDN11) ENSP00000417434.1:n.391+60485_391+60486delinsCA
NM_020949.2:c.907-291_907-290delinsTG (SLC7A14) NP_066000.2:n.907-291_907-290delinsTG
XM_011513058.1:c.-21-291_-21-290delinsTG (SLC7A14) XP_011511360.1:n.-21-291_-21-290delinsTG
NR_135555.1:n.215+6939_215+6940delinsCA (SLC7A14-AS1)
NR_135556.1:n.215+6939_215+6940delinsCA (SLC7A14-AS1)
NR_135557.1:n.221+6939_221+6940delinsCA (SLC7A14-AS1)
NM_020949.3:c.907-291_907-290delinsTG (SLC7A14) MANE Select NP_066000.2:n.907-291_907-290delinsTG