Canonical Allele Identifier: CA343307461

Gene: ITLN1

Linked Data

• MyVariant Identifiers: chr1:g.160851950T>G (hg19) ; chr1:g.160882160T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160882160T>G , CM000663.2:g.160882160T>G	GRCh38
NC_000001.10:g.160851950T>G , CM000663.1:g.160851950T>G	GRCh37
NC_000001.9:g.159118574T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000326245.4:c.202A>C MANE Select	ENSP00000323587.3:p.Thr68Pro
ENST00000326245.3:c.202A>C	ENSP00000323587.3:p.Thr68Pro
ENST00000464077.1:n.136A>C
NM_017625.2:c.202A>C	NP_060095.2:p.Thr68Pro
NM_017625.3:c.202A>C MANE Select	NP_060095.2:p.Thr68Pro