Canonical Allele Identifier: CA1144150042
Gene: ITLN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160882569A= , CM000663.2:g.160882569A= GRCh38
NC_000001.10:g.160852359A= , CM000663.1:g.160852359A= GRCh37
NC_000001.9:g.159118983A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326245.4:c.158-365T= MANE Select ENSP00000323587.3:n.158-365T=
ENST00000326245.3:c.158-365T= ENSP00000323587.3:n.158-365T=
NM_017625.2:c.158-365T= NP_060095.2:n.158-365T=
NM_017625.3:c.158-365T= MANE Select NP_060095.2:n.158-365T=
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