Canonical Allele Identifier: CA890140151
Gene: ITLN1 HGNC NCBI

Linked Data

dbSNP Id: rs1425419525
MyVariant Identifiers: chr1:g.160852405_160852406insTGG (hg19) chr1:g.160882615_160882616insTGG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160882618_160882620dup , CM000663.2:g.160882618_160882620dup GRCh38
NC_000001.10:g.160852408_160852410dup , CM000663.1:g.160852408_160852410dup GRCh37
NC_000001.9:g.159119032_159119034dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326245.4:c.158-414_158-412dup MANE Select ENSP00000323587.3:n.158-414_158-412dup
ENST00000326245.3:c.158-414_158-412dup ENSP00000323587.3:n.158-414_158-412dup
NM_017625.2:c.158-414_158-412dup NP_060095.2:n.158-414_158-412dup
NM_017625.3:c.158-414_158-412dup MANE Select NP_060095.2:n.158-414_158-412dup
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