Canonical Allele Identifier: CA890138710

Gene: ITLN1

Linked Data

• dbSNP Id: rs1399299332
• MyVariant Identifiers: chr1:g.160851583_160851588del (hg19) ; chr1:g.160881793_160881798del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160881796_160881801del , CM000663.2:g.160881796_160881801del	GRCh38
NC_000001.10:g.160851586_160851591del , CM000663.1:g.160851586_160851591del	GRCh37
NC_000001.9:g.159118210_159118215del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326245.4:c.405+159_405+164del MANE Select	ENSP00000323587.3:n.405+159_405+164del
ENST00000326245.3:c.405+159_405+164del	ENSP00000323587.3:n.405+159_405+164del
ENST00000464077.1:n.339+159_339+164del
NM_017625.2:c.405+159_405+164del	NP_060095.2:n.405+159_405+164del
NM_017625.3:c.405+159_405+164del MANE Select	NP_060095.2:n.405+159_405+164del