Canonical Allele Identifier: CA2674827732
Gene: TSLP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071712_111071713insTCCCTG , CM000667.2:g.111071712_111071713insTCCCTG GRCh38
NC_000005.9:g.110407410_110407411insTCCCTG , CM000667.1:g.110407410_110407411insTCCCTG GRCh37
NC_000005.8:g.110435309_110435310insTCCCTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-178-1_-178insTCCCTG MANE Select ENSP00000339804.3:n.-178-1_-178insTCCCTG
ENST00000344895.3:c.-179_-178insTCCCTG ENSP00000339804.3:n.-179_-178insTCCCTG
ENST00000420978.6:c.34+195_34+196insTCCCTG ENSP00000399099.2:n.34+195_34+196insTCCCTG
NM_033035.4:c.-179_-178insTCCCTG NP_149024.1:n.-179_-178insTCCCTG
NR_045089.1:n.1438+195_1438+196insTCCCTG
NM_033035.5:c.-178-1_-178insTCCCTG MANE Select NP_149024.1:n.-178-1_-178insTCCCTG
NR_045089.2:n.1456+195_1456+196insTCCCTG