Canonical Allele Identifier: CA360602491

Gene: TSLP

Linked Data

• MyVariant Identifiers: chr5:g.110407642C>G (hg19) ; chr5:g.111071944C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111071944C>G , CM000667.2:g.111071944C>G	GRCh38
NC_000005.9:g.110407642C>G , CM000667.1:g.110407642C>G	GRCh37
NC_000005.8:g.110435541C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344895.4:c.54C>G MANE Select	ENSP00000339804.3:p.Phe18Leu
ENST00000344895.3:c.54C>G	ENSP00000339804.3:p.Phe18Leu
ENST00000420978.6:c.54C>G	ENSP00000399099.2:p.Phe18Leu
NM_033035.4:c.54C>G	NP_149024.1:p.Phe18Leu
NR_045089.1:n.1458C>G
NM_033035.5:c.54C>G MANE Select	NP_149024.1:p.Phe18Leu
NR_045089.2:n.1476C>G