Canonical Allele Identifier: CA2674827753
Gene: TSLP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071738_111071740dup , CM000667.2:g.111071738_111071740dup GRCh38
NC_000005.9:g.110407436_110407438dup , CM000667.1:g.110407436_110407438dup GRCh37
NC_000005.8:g.110435335_110435337dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-153_-151dup MANE Select ENSP00000339804.3:n.-153_-151dup
ENST00000344895.3:c.-153_-151dup ENSP00000339804.3:n.-153_-151dup
ENST00000420978.6:c.35-187_35-185dup ENSP00000399099.2:n.35-187_35-185dup
NM_033035.4:c.-153_-151dup NP_149024.1:n.-153_-151dup
NR_045089.1:n.1439-187_1439-185dup
NM_033035.5:c.-153_-151dup MANE Select NP_149024.1:n.-153_-151dup
NR_045089.2:n.1457-187_1457-185dup