Canonical Allele Identifier: CA1572623259
Gene: TSLP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111077896A= , CM000667.2:g.111077896A= GRCh38
NC_000005.9:g.110413594A= , CM000667.1:g.110413594A= GRCh37
NC_000005.8:g.110441493A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.*1822A= MANE Select ENSP00000339804.3:n.*1822A=
ENST00000379706.4:c.*1822A= ENSP00000427827.1:n.*1822A=
NM_033035.4:c.*1822A= NP_149024.1:n.*1822A=
NM_138551.4:c.*1822A= NP_612561.2:n.*1822A=
NR_045089.1:n.3706A=
NM_033035.5:c.*1822A= MANE Select NP_149024.1:n.*1822A=
NM_138551.5:c.*1822A= NP_612561.2:n.*1822A=
NR_045089.2:n.3724A=