Canonical Allele Identifier: CA2538642609
Gene: TSLP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071802_111071803insT , CM000667.2:g.111071802_111071803insT GRCh38
NC_000005.9:g.110407500_110407501insT , CM000667.1:g.110407500_110407501insT GRCh37
NC_000005.8:g.110435399_110435400insT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-89_-88insT MANE Select ENSP00000339804.3:n.-89_-88insT
ENST00000344895.3:c.-89_-88insT ENSP00000339804.3:n.-89_-88insT
ENST00000420978.6:c.35-123_35-122insT ENSP00000399099.2:n.35-123_35-122insT
NM_033035.4:c.-89_-88insT NP_149024.1:n.-89_-88insT
NR_045089.1:n.1439-123_1439-122insT
NM_033035.5:c.-89_-88insT MANE Select NP_149024.1:n.-89_-88insT
NR_045089.2:n.1457-123_1457-122insT