Canonical Allele Identifier: CA1572622483
Gene: TSLP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111077112A= , CM000667.2:g.111077112A= GRCh38
NC_000005.9:g.110412810A= , CM000667.1:g.110412810A= GRCh37
NC_000005.8:g.110440709A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000344895.4:c.*1038A= MANE Select ENSP00000339804.3:n.*1038A=
ENST00000379706.4:c.*1038A= ENSP00000427827.1:n.*1038A=
NM_033035.4:c.*1038A= NP_149024.1:n.*1038A=
NM_138551.4:c.*1038A= NP_612561.2:n.*1038A=
NR_045089.1:n.2922A=
NM_033035.5:c.*1038A= MANE Select NP_149024.1:n.*1038A=
NM_138551.5:c.*1038A= NP_612561.2:n.*1038A=
NR_045089.2:n.2940A=