Canonical Allele Identifier: CA2674829060
Gene: TSLP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111077243C>T , CM000667.2:g.111077243C>T GRCh38
NC_000005.9:g.110412941C>T , CM000667.1:g.110412941C>T GRCh37
NC_000005.8:g.110440840C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.*1169C>T MANE Select ENSP00000339804.3:n.*1169C>T
ENST00000379706.4:c.*1169C>T ENSP00000427827.1:n.*1169C>T
NM_033035.4:c.*1169C>T NP_149024.1:n.*1169C>T
NM_138551.4:c.*1169C>T NP_612561.2:n.*1169C>T
NR_045089.1:n.3053C>T
NM_033035.5:c.*1169C>T MANE Select NP_149024.1:n.*1169C>T
NM_138551.5:c.*1169C>T NP_612561.2:n.*1169C>T
NR_045089.2:n.3071C>T