Canonical Allele Identifier: CA1572617367
Gene: TSLP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111072488T= , CM000667.2:g.111072488T= GRCh38
NC_000005.9:g.110408186T= , CM000667.1:g.110408186T= GRCh37
NC_000005.8:g.110436085T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.172-400T= MANE Select ENSP00000339804.3:n.172-400T=
ENST00000344895.3:c.172-400T= ENSP00000339804.3:n.172-400T=
ENST00000420978.6:c.172-400T= ENSP00000399099.2:n.172-400T=
NM_033035.4:c.172-400T= NP_149024.1:n.172-400T=
NR_045089.1:n.1576-400T=
NM_033035.5:c.172-400T= MANE Select NP_149024.1:n.172-400T=
NR_045089.2:n.1594-400T=