Canonical Allele Identifier: CA1572617377
Gene: TSLP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111072501_111072502delinsAT , CM000667.2:g.111072501_111072502delinsAT GRCh38
NC_000005.9:g.110408199_110408200delinsAT , CM000667.1:g.110408199_110408200delinsAT GRCh37
NC_000005.8:g.110436098_110436099delinsAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.172-387_172-386delinsAT MANE Select ENSP00000339804.3:n.172-387_172-386delinsAT
ENST00000344895.3:c.172-387_172-386delinsAT ENSP00000339804.3:n.172-387_172-386delinsAT
ENST00000420978.6:c.172-387_172-386delinsAT ENSP00000399099.2:n.172-387_172-386delinsAT
NM_033035.4:c.172-387_172-386delinsAT NP_149024.1:n.172-387_172-386delinsAT
NR_045089.1:n.1576-387_1576-386delinsAT
NM_033035.5:c.172-387_172-386delinsAT MANE Select NP_149024.1:n.172-387_172-386delinsAT
NR_045089.2:n.1594-387_1594-386delinsAT
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