Canonical Allele Identifier: CA1572617249
Gene: TSLP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111072337_111072338delinsAC , CM000667.2:g.111072337_111072338delinsAC GRCh38
NC_000005.9:g.110408035_110408036delinsAC , CM000667.1:g.110408035_110408036delinsAC GRCh37
NC_000005.8:g.110435934_110435935delinsAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.171+276_171+277delinsAC MANE Select ENSP00000339804.3:n.171+276_171+277delinsAC
ENST00000344895.3:c.171+276_171+277delinsAC ENSP00000339804.3:n.171+276_171+277delinsAC
ENST00000420978.6:c.171+276_171+277delinsAC ENSP00000399099.2:n.171+276_171+277delinsAC
NM_033035.4:c.171+276_171+277delinsAC NP_149024.1:n.171+276_171+277delinsAC
NR_045089.1:n.1575+276_1575+277delinsAC
NM_033035.5:c.171+276_171+277delinsAC MANE Select NP_149024.1:n.171+276_171+277delinsAC
NR_045089.2:n.1593+276_1593+277delinsAC