Canonical Allele Identifier: CA1141614173
Gene: ITLN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160882091G= , CM000663.2:g.160882091G= GRCh38
NC_000001.10:g.160851881G= , CM000663.1:g.160851881G= GRCh37
NC_000001.9:g.159118505G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326245.4:c.271C= MANE Select ENSP00000323587.3:p.Arg91=
ENST00000326245.3:c.271C= ENSP00000323587.3:p.Arg91=
ENST00000464077.1:n.205C=
NM_017625.2:c.271C= NP_060095.2:p.Arg91=
NM_017625.3:c.271C= MANE Select NP_060095.2:p.Arg91=
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