Canonical Allele Identifier: CA527133862
Gene: ITLN1 HGNC NCBI

Linked Data

dbSNP Id: rs1415950104
gnomAD v2: 1-160851590-TCAAGAAA-T
gnomAD v3: 1-160881800-TCAAGAAA-T
gnomAD v4: 1-160881800-TCAAGAAA-T
MyVariant Identifiers: chr1:g.160851591_160851597del (hg19) chr1:g.160881801_160881807del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160881801_160881807del , CM000663.2:g.160881801_160881807del GRCh38
NC_000001.10:g.160851591_160851597del , CM000663.1:g.160851591_160851597del GRCh37
NC_000001.9:g.159118215_159118221del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326245.4:c.405+150_405+156del MANE Select ENSP00000323587.3:n.405+150_405+156del
ENST00000326245.3:c.405+150_405+156del ENSP00000323587.3:n.405+150_405+156del
ENST00000464077.1:n.339+150_339+156del
NM_017625.2:c.405+150_405+156del NP_060095.2:n.405+150_405+156del
NM_017625.3:c.405+150_405+156del MANE Select NP_060095.2:n.405+150_405+156del
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