Canonical Allele Identifier: CA343307178

Gene: ITLN1

Linked Data

• MyVariant Identifiers: chr1:g.160851816C>A (hg19) ; chr1:g.160882026C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160882026C>A , CM000663.2:g.160882026C>A	GRCh38
NC_000001.10:g.160851816C>A , CM000663.1:g.160851816C>A	GRCh37
NC_000001.9:g.159118440C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326245.4:c.336G>T MANE Select	ENSP00000323587.3:p.Glu112Asp
ENST00000326245.3:c.336G>T	ENSP00000323587.3:p.Glu112Asp
ENST00000464077.1:n.270G>T
NM_017625.2:c.336G>T	NP_060095.2:p.Glu112Asp
NM_017625.3:c.336G>T MANE Select	NP_060095.2:p.Glu112Asp