Canonical Allele Identifier: CA1572616649
Gene: TSLP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071891A= , CM000667.2:g.111071891A= GRCh38
NC_000005.9:g.110407589A= , CM000667.1:g.110407589A= GRCh37
NC_000005.8:g.110435488A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.1A= MANE Select ENSP00000339804.3:p.Met1=
ENST00000344895.3:c.1A= ENSP00000339804.3:p.Met1=
ENST00000420978.6:c.35-34A= ENSP00000399099.2:n.35-34A=
NM_033035.4:c.1A= NP_149024.1:p.Met1=
NR_045089.1:n.1439-34A=
NM_033035.5:c.1A= MANE Select NP_149024.1:p.Met1=
NR_045089.2:n.1457-34A=