Canonical Allele Identifier: CA1572622491
Gene: TSLP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111077119G= , CM000667.2:g.111077119G= GRCh38
NC_000005.9:g.110412817G= , CM000667.1:g.110412817G= GRCh37
NC_000005.8:g.110440716G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000344895.4:c.*1045G= MANE Select ENSP00000339804.3:n.*1045G=
ENST00000379706.4:c.*1045G= ENSP00000427827.1:n.*1045G=
NM_033035.4:c.*1045G= NP_149024.1:n.*1045G=
NM_138551.4:c.*1045G= NP_612561.2:n.*1045G=
NR_045089.1:n.2929G=
NM_033035.5:c.*1045G= MANE Select NP_149024.1:n.*1045G=
NM_138551.5:c.*1045G= NP_612561.2:n.*1045G=
NR_045089.2:n.2947G=