Canonical Allele Identifier: CA343307477

Gene: ITLN1

Linked Data

• COSMIC: COSM75049
• MyVariant Identifiers: chr1:g.160851956A>T (hg19) ; chr1:g.160882166A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160882166A>T , CM000663.2:g.160882166A>T	GRCh38
NC_000001.10:g.160851956A>T , CM000663.1:g.160851956A>T	GRCh37
NC_000001.9:g.159118580A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000326245.4:c.196T>A MANE Select	ENSP00000323587.3:p.Tyr66Asn
ENST00000326245.3:c.196T>A	ENSP00000323587.3:p.Tyr66Asn
ENST00000464077.1:n.130T>A
NM_017625.2:c.196T>A	NP_060095.2:p.Tyr66Asn
NM_017625.3:c.196T>A MANE Select	NP_060095.2:p.Tyr66Asn