Canonical Allele Identifier: CA650193679
Gene: TSLP HGNC NCBI

Linked Data

COSMIC: COSN21368205
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111077125G>T , CM000667.2:g.111077125G>T GRCh38
NC_000005.9:g.110412823G>T , CM000667.1:g.110412823G>T GRCh37
NC_000005.8:g.110440722G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000344895.4:c.*1051G>T MANE Select ENSP00000339804.3:n.*1051G>T
ENST00000379706.4:c.*1051G>T ENSP00000427827.1:n.*1051G>T
NM_033035.4:c.*1051G>T NP_149024.1:n.*1051G>T
NM_138551.4:c.*1051G>T NP_612561.2:n.*1051G>T
NR_045089.1:n.2935G>T
NM_033035.5:c.*1051G>T MANE Select NP_149024.1:n.*1051G>T
NM_138551.5:c.*1051G>T NP_612561.2:n.*1051G>T
NR_045089.2:n.2953G>T
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