Canonical Allele Identifier: CA1572617353
Gene: TSLP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111072471_111072475delinsCTATT , CM000667.2:g.111072471_111072475delinsCTATT GRCh38
NC_000005.9:g.110408169_110408173delinsCTATT , CM000667.1:g.110408169_110408173delinsCTATT GRCh37
NC_000005.8:g.110436068_110436072delinsCTATT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.171+410_172-413delinsCTATT MANE Select ENSP00000339804.3:n.171+410_172-413delinsCTATT
ENST00000344895.3:c.171+410_172-413delinsCTATT ENSP00000339804.3:n.171+410_172-413delinsCTATT
ENST00000420978.6:c.171+410_172-413delinsCTATT ENSP00000399099.2:n.171+410_172-413delinsCTATT
NM_033035.4:c.171+410_172-413delinsCTATT NP_149024.1:n.171+410_172-413delinsCTATT
NR_045089.1:n.1575+410_1576-413delinsCTATT
NM_033035.5:c.171+410_172-413delinsCTATT MANE Select NP_149024.1:n.171+410_172-413delinsCTATT
NR_045089.2:n.1593+410_1594-413delinsCTATT