Canonical Allele Identifier: CA650193740

Gene: TSLP

Linked Data

• dbSNP Id: rs1305917986
• gnomAD v3: 5-111077968-G-A
• gnomAD v4: 5-111077968-G-A
• COSMIC: COSN21922927
• MyVariant Identifiers: chr5:g.110413666G>A (hg19) ; chr5:g.111077968G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111077968G>A , CM000667.2:g.111077968G>A	GRCh38
NC_000005.9:g.110413666G>A , CM000667.1:g.110413666G>A	GRCh37
NC_000005.8:g.110441565G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000344895.4:c.*1894G>A MANE Select	ENSP00000339804.3:n.*1894G>A
ENST00000379706.4:c.*1894G>A	ENSP00000427827.1:n.*1894G>A
NM_033035.4:c.*1894G>A	NP_149024.1:n.*1894G>A
NM_138551.4:c.*1894G>A	NP_612561.2:n.*1894G>A
NR_045089.1:n.3778G>A
NM_033035.5:c.*1894G>A MANE Select	NP_149024.1:n.*1894G>A
NM_138551.5:c.*1894G>A	NP_612561.2:n.*1894G>A
NR_045089.2:n.3796G>A