Canonical Allele Identifier: CA1143521377
Gene: ITLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160881972C= , CM000663.2:g.160881972C= GRCh38
NC_000001.10:g.160851762C= , CM000663.1:g.160851762C= GRCh37
NC_000001.9:g.159118386C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326245.4:c.390G= MANE Select ENSP00000323587.3:p.Thr130=
ENST00000326245.3:c.390G= ENSP00000323587.3:p.Thr130=
ENST00000464077.1:n.324G=
NM_017625.2:c.390G= NP_060095.2:p.Thr130=
NM_017625.3:c.390G= MANE Select NP_060095.2:p.Thr130=