Canonical Allele Identifier: CA526865827
Gene: ITLN1 HGNC NCBI

Linked Data

dbSNP Id: rs1299463259
gnomAD v2: 1-160852138-TG-T
gnomAD v3: 1-160882348-TG-T
gnomAD v4: 1-160882348-TG-T
MyVariant Identifiers: chr1:g.160852139del (hg19) chr1:g.160882349del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160882352del , CM000663.2:g.160882352del GRCh38
NC_000001.10:g.160852142del , CM000663.1:g.160852142del GRCh37
NC_000001.9:g.159118766del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326245.4:c.158-145del MANE Select ENSP00000323587.3:n.158-145del
ENST00000326245.3:c.158-145del ENSP00000323587.3:n.158-145del
NM_017625.2:c.158-145del NP_060095.2:n.158-145del
NM_017625.3:c.158-145del MANE Select NP_060095.2:n.158-145del
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