Canonical Allele Identifier: CA1080102210
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1752342001

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071738_111071743del , CM000667.2:g.111071738_111071743del GRCh38
NC_000005.9:g.110407436_110407441del , CM000667.1:g.110407436_110407441del GRCh37
NC_000005.8:g.110435335_110435340del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-153_-148del MANE Select ENSP00000339804.3:n.-153_-148del
ENST00000344895.3:c.-153_-148del ENSP00000339804.3:n.-153_-148del
ENST00000420978.6:c.35-187_35-182del ENSP00000399099.2:n.35-187_35-182del
NM_033035.4:c.-153_-148del NP_149024.1:n.-153_-148del
NR_045089.1:n.1439-187_1439-182del
NM_033035.5:c.-153_-148del MANE Select NP_149024.1:n.-153_-148del
NR_045089.2:n.1457-187_1457-182del