Canonical Allele Identifier: CA124874220
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs575595021
gnomAD v2: 5-110408169-CTATT-C
gnomAD v3: 5-111072471-CTATT-C
gnomAD v4: 5-111072471-CTATT-C
MyVariant Identifiers: chr5:g.110408170_110408173del (hg19) chr5:g.111072472_111072475del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111072476_111072479del , CM000667.2:g.111072476_111072479del GRCh38
NC_000005.9:g.110408174_110408177del , CM000667.1:g.110408174_110408177del GRCh37
NC_000005.8:g.110436073_110436076del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.172-412_172-409del MANE Select ENSP00000339804.3:n.172-412_172-409del
ENST00000344895.3:c.172-412_172-409del ENSP00000339804.3:n.172-412_172-409del
ENST00000420978.6:c.172-412_172-409del ENSP00000399099.2:n.172-412_172-409del
NM_033035.4:c.172-412_172-409del NP_149024.1:n.172-412_172-409del
NR_045089.1:n.1576-412_1576-409del
NM_033035.5:c.172-412_172-409del MANE Select NP_149024.1:n.172-412_172-409del
NR_045089.2:n.1594-412_1594-409del
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