Canonical Allele Identifier: CA360602479

Gene: TSLP

Linked Data

• MyVariant Identifiers: chr5:g.110407637A>T (hg19) ; chr5:g.111071939A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111071939A>T , CM000667.2:g.111071939A>T	GRCh38
NC_000005.9:g.110407637A>T , CM000667.1:g.110407637A>T	GRCh37
NC_000005.8:g.110435536A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344895.4:c.49A>T MANE Select	ENSP00000339804.3:p.Ile17Phe
ENST00000344895.3:c.49A>T	ENSP00000339804.3:p.Ile17Phe
ENST00000420978.6:c.49A>T	ENSP00000399099.2:p.Ile17Phe
NM_033035.4:c.49A>T	NP_149024.1:p.Ile17Phe
NR_045089.1:n.1453A>T
NM_033035.5:c.49A>T MANE Select	NP_149024.1:p.Ile17Phe
NR_045089.2:n.1471A>T