Canonical Allele Identifier: CA1202506141
Gene: ITLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160881677T= , CM000663.2:g.160881677T= GRCh38
NC_000001.10:g.160851467T= , CM000663.1:g.160851467T= GRCh37
NC_000001.9:g.159118091T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326245.4:c.405+280A= MANE Select ENSP00000323587.3:n.405+280A=
ENST00000326245.3:c.405+280A= ENSP00000323587.3:n.405+280A=
ENST00000464077.1:n.339+280A=
NM_017625.2:c.405+280A= NP_060095.2:n.405+280A=
NM_017625.3:c.405+280A= MANE Select NP_060095.2:n.405+280A=