Canonical Allele Identifier: CA890140028

Gene: ITLN1

Linked Data

• dbSNP Id: rs1175832803
• MyVariant Identifiers: chr1:g.160852241_160852242insT (hg19) ; chr1:g.160882451_160882452insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160882453dup , CM000663.2:g.160882453dup	GRCh38
NC_000001.10:g.160852243dup , CM000663.1:g.160852243dup	GRCh37
NC_000001.9:g.159118867dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326245.4:c.158-248dup MANE Select	ENSP00000323587.3:n.158-248dup
ENST00000326245.3:c.158-248dup	ENSP00000323587.3:n.158-248dup
NM_017625.2:c.158-248dup	NP_060095.2:n.158-248dup
NM_017625.3:c.158-248dup MANE Select	NP_060095.2:n.158-248dup