Canonical Allele Identifier: CA2709813565
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs2112551028
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111077900_111077902del , CM000667.2:g.111077900_111077902del GRCh38
NC_000005.9:g.110413598_110413600del , CM000667.1:g.110413598_110413600del GRCh37
NC_000005.8:g.110441497_110441499del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.*1826_*1828del MANE Select ENSP00000339804.3:n.*1826_*1828del
ENST00000379706.4:c.*1826_*1828del ENSP00000427827.1:n.*1826_*1828del
NM_033035.4:c.*1826_*1828del NP_149024.1:n.*1826_*1828del
NM_138551.4:c.*1826_*1828del NP_612561.2:n.*1826_*1828del
NR_045089.1:n.3710_3712del
NM_033035.5:c.*1826_*1828del MANE Select NP_149024.1:n.*1826_*1828del
NM_138551.5:c.*1826_*1828del NP_612561.2:n.*1826_*1828del
NR_045089.2:n.3728_3730del
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