Canonical Allele Identifier: CA343307158

Gene: ITLN1

Linked Data

• MyVariant Identifiers: chr1:g.160851806T>C (hg19) ; chr1:g.160882016T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160882016T>C , CM000663.2:g.160882016T>C	GRCh38
NC_000001.10:g.160851806T>C , CM000663.1:g.160851806T>C	GRCh37
NC_000001.9:g.159118430T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326245.4:c.346A>G MANE Select	ENSP00000323587.3:p.Asn116Asp
ENST00000326245.3:c.346A>G	ENSP00000323587.3:p.Asn116Asp
ENST00000464077.1:n.280A>G
NM_017625.2:c.346A>G	NP_060095.2:p.Asn116Asp
NM_017625.3:c.346A>G MANE Select	NP_060095.2:p.Asn116Asp