Canonical Allele Identifier: CA421604961
Gene: ITLN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.160851777A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160881987A>T , CM000663.2:g.160881987A>T GRCh38
NC_000001.10:g.160851777A>T , CM000663.1:g.160851777A>T GRCh37
NC_000001.9:g.159118401A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326245.4:c.375T>A MANE Select ENSP00000323587.3:p.Ser125=
ENST00000326245.3:c.375T>A ENSP00000323587.3:p.Ser125=
ENST00000464077.1:n.309T>A
NM_017625.2:c.375T>A NP_060095.2:p.Ser125=
NM_017625.3:c.375T>A MANE Select NP_060095.2:p.Ser125=