Canonical Allele Identifier: CA1572617363
Gene: TSLP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111072480_111072481delinsAC , CM000667.2:g.111072480_111072481delinsAC GRCh38
NC_000005.9:g.110408178_110408179delinsAC , CM000667.1:g.110408178_110408179delinsAC GRCh37
NC_000005.8:g.110436077_110436078delinsAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.172-408_172-407delinsAC MANE Select ENSP00000339804.3:n.172-408_172-407delinsAC
ENST00000344895.3:c.172-408_172-407delinsAC ENSP00000339804.3:n.172-408_172-407delinsAC
ENST00000420978.6:c.172-408_172-407delinsAC ENSP00000399099.2:n.172-408_172-407delinsAC
NM_033035.4:c.172-408_172-407delinsAC NP_149024.1:n.172-408_172-407delinsAC
NR_045089.1:n.1576-408_1576-407delinsAC
NM_033035.5:c.172-408_172-407delinsAC MANE Select NP_149024.1:n.172-408_172-407delinsAC
NR_045089.2:n.1594-408_1594-407delinsAC