Canonical Allele Identifier: CA3364869
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs760053269

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071929_111071932del , CM000667.2:g.111071929_111071932del GRCh38
NC_000005.9:g.110407627_110407630del , CM000667.1:g.110407627_110407630del GRCh37
NC_000005.8:g.110435526_110435529del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.39_42del MANE Select ENSP00000339804.3:p.Phe14GlyfsTer9
ENST00000344895.3:c.39_42del ENSP00000339804.3:p.Phe14GlyfsTer9
ENST00000420978.6:c.39_42del ENSP00000399099.2:p.Phe14GlyfsTer9
NM_033035.4:c.39_42del NP_149024.1:p.Phe14GlyfsTer9
NR_045089.1:n.1443_1446del
NM_033035.5:c.39_42del MANE Select NP_149024.1:p.Phe14GlyfsTer9
NR_045089.2:n.1461_1464del