Canonical Allele Identifier: CA2759362262

Gene: SLC7A14 CLDN11 SLC7A14-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.170483645_170483646insAGA , CM000665.2:g.170483645_170483646insAGA	GRCh38
NC_000003.11:g.170201434_170201435insAGA , CM000665.1:g.170201434_170201435insAGA	GRCh37
NC_000003.10:g.171684128_171684129insAGA	NCBI36
NG_034121.1:g.107429_107430insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231706.6:c.907-124_907-123insTCT (SLC7A14) MANE Select	ENSP00000231706.4:n.907-124_907-123insTCT
ENST00000231706.5:c.907-124_907-123insTCT (SLC7A14)	ENSP00000231706.4:n.907-124_907-123insTCT
ENST00000471373.5:n.373-19166_373-19165insAGA (CLDN11)
ENST00000480067.1:n.218+6772_218+6773insAGA (CLDN11)
ENST00000486975.1:c.391+60318_391+60319insAGA (CLDN11)	ENSP00000417434.1:n.391+60318_391+60319insAGA
NM_020949.2:c.907-124_907-123insTCT (SLC7A14)	NP_066000.2:n.907-124_907-123insTCT
XM_011513058.1:c.-21-124_-21-123insTCT (SLC7A14)	XP_011511360.1:n.-21-124_-21-123insTCT
NR_135555.1:n.215+6772_215+6773insAGA (SLC7A14-AS1)
NR_135556.1:n.215+6772_215+6773insAGA (SLC7A14-AS1)
NR_135557.1:n.221+6772_221+6773insAGA (SLC7A14-AS1)
NM_020949.3:c.907-124_907-123insTCT (SLC7A14) MANE Select	NP_066000.2:n.907-124_907-123insTCT