Canonical Allele Identifier: CA1572617163
Gene: TSLP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111072283A= , CM000667.2:g.111072283A= GRCh38
NC_000005.9:g.110407981A= , CM000667.1:g.110407981A= GRCh37
NC_000005.8:g.110435880A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.171+222A= MANE Select ENSP00000339804.3:n.171+222A=
ENST00000344895.3:c.171+222A= ENSP00000339804.3:n.171+222A=
ENST00000420978.6:c.171+222A= ENSP00000399099.2:n.171+222A=
NM_033035.4:c.171+222A= NP_149024.1:n.171+222A=
NR_045089.1:n.1575+222A=
NM_033035.5:c.171+222A= MANE Select NP_149024.1:n.171+222A=
NR_045089.2:n.1593+222A=
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