Canonical Allele Identifier: CA1143970369
Gene: ITLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160881963G= , CM000663.2:g.160881963G= GRCh38
NC_000001.10:g.160851753G= , CM000663.1:g.160851753G= GRCh37
NC_000001.9:g.159118377G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000326245.4:c.399C= MANE Select ENSP00000323587.3:p.Asp133=
ENST00000326245.3:c.399C= ENSP00000323587.3:p.Asp133=
ENST00000464077.1:n.333C=
NM_017625.2:c.399C= NP_060095.2:p.Asp133=
NM_017625.3:c.399C= MANE Select NP_060095.2:p.Asp133=