Canonical Allele Identifier: CA1202506257
Gene: ITLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160881860C= , CM000663.2:g.160881860C= GRCh38
NC_000001.10:g.160851650C= , CM000663.1:g.160851650C= GRCh37
NC_000001.9:g.159118274C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326245.4:c.405+97G= MANE Select ENSP00000323587.3:n.405+97G=
ENST00000326245.3:c.405+97G= ENSP00000323587.3:n.405+97G=
ENST00000464077.1:n.339+97G=
NM_017625.2:c.405+97G= NP_060095.2:n.405+97G=
NM_017625.3:c.405+97G= MANE Select NP_060095.2:n.405+97G=