Canonical Allele Identifier: CA1572616586
Gene: TSLP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071850A= , CM000667.2:g.111071850A= GRCh38
NC_000005.9:g.110407548A= , CM000667.1:g.110407548A= GRCh37
NC_000005.8:g.110435447A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-41A= MANE Select ENSP00000339804.3:n.-41A=
ENST00000344895.3:c.-41A= ENSP00000339804.3:n.-41A=
ENST00000420978.6:c.35-75A= ENSP00000399099.2:n.35-75A=
NM_033035.4:c.-41A= NP_149024.1:n.-41A=
NR_045089.1:n.1439-75A=
NM_033035.5:c.-41A= MANE Select NP_149024.1:n.-41A=
NR_045089.2:n.1457-75A=