Canonical Allele Identifier: CA1572617300
Gene: TSLP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111072390_111072392delinsAAG , CM000667.2:g.111072390_111072392delinsAAG GRCh38
NC_000005.9:g.110408088_110408090delinsAAG , CM000667.1:g.110408088_110408090delinsAAG GRCh37
NC_000005.8:g.110435987_110435989delinsAAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.171+329_171+331delinsAAG MANE Select ENSP00000339804.3:n.171+329_171+331delinsAAG
ENST00000344895.3:c.171+329_171+331delinsAAG ENSP00000339804.3:n.171+329_171+331delinsAAG
ENST00000420978.6:c.171+329_171+331delinsAAG ENSP00000399099.2:n.171+329_171+331delinsAAG
NM_033035.4:c.171+329_171+331delinsAAG NP_149024.1:n.171+329_171+331delinsAAG
NR_045089.1:n.1575+329_1575+331delinsAAG
NM_033035.5:c.171+329_171+331delinsAAG MANE Select NP_149024.1:n.171+329_171+331delinsAAG
NR_045089.2:n.1593+329_1593+331delinsAAG