Canonical Allele Identifier: CA1202506343
Gene: ITLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160882068A= , CM000663.2:g.160882068A= GRCh38
NC_000001.10:g.160851858A= , CM000663.1:g.160851858A= GRCh37
NC_000001.9:g.159118482A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326245.4:c.294T= MANE Select ENSP00000323587.3:p.Asp98=
ENST00000326245.3:c.294T= ENSP00000323587.3:p.Asp98=
ENST00000464077.1:n.228T=
NM_017625.2:c.294T= NP_060095.2:p.Asp98=
NM_017625.3:c.294T= MANE Select NP_060095.2:p.Asp98=