Canonical Allele Identifier: CA1572623231
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1752555284

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111077864_111077875del , CM000667.2:g.111077864_111077875del GRCh38
NC_000005.9:g.110413562_110413573del , CM000667.1:g.110413562_110413573del GRCh37
NC_000005.8:g.110441461_110441472del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000344895.4:c.*1790_*1801del MANE Select ENSP00000339804.3:n.*1790_*1801del
ENST00000379706.4:c.*1790_*1801del ENSP00000427827.1:n.*1790_*1801del
NM_033035.4:c.*1790_*1801del NP_149024.1:n.*1790_*1801del
NM_138551.4:c.*1790_*1801del NP_612561.2:n.*1790_*1801del
NR_045089.1:n.3674_3685del
NM_033035.5:c.*1790_*1801del MANE Select NP_149024.1:n.*1790_*1801del
NM_138551.5:c.*1790_*1801del NP_612561.2:n.*1790_*1801del
NR_045089.2:n.3692_3703del