Canonical Allele Identifier: CA2650221023

Gene: IL19

Linked Data

• gnomAD v4: 1-206842613-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206842614del , CM000663.2:g.206842614del	GRCh38
NC_000001.10:g.207015959del , CM000663.1:g.207015959del	GRCh37
NC_000001.9:g.205082582del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000659997.3:c.526del MANE Select	ENSP00000499459.2:p.Ser176GlnfsTer9
ENST00000340758.7:c.526del	ENSP00000343000.3:p.Ser176GlnfsTer9
ENST00000656872.2:c.526del	ENSP00000499487.2:p.Ser176GlnfsTer9
ENST00000659997.2:c.526del	ENSP00000499459.2:p.Ser176GlnfsTer9
ENST00000270218.10:c.526del	ENSP00000270218.6:p.Ser176GlnfsTer?
ENST00000340758.6:c.640del	ENSP00000343000.2:p.Ser214GlnfsTer9
ENST00000620365.1:c.526del	ENSP00000482668.1:p.Ser176GlnfsTer9
NM_013371.3:c.526del	NP_037503.2:p.Ser176GlnfsTer9
NM_153758.2:c.640del	NP_715639.1:p.Ser214GlnfsTer9
XR_922482.1:n.208del
XR_922482.2:n.208del
NM_001369605.1:c.526del	NP_001356534.1:p.Ser176GlnfsTer9
NM_153758.3:c.640del	NP_715639.1:p.Ser214GlnfsTer9
NM_001393490.1:c.526del	NP_001380419.1:p.Ser176GlnfsTer9
NM_001393491.1:c.526del	NP_001380420.1:p.Ser176GlnfsTer9
NM_013371.5:c.526del	NP_037503.2:p.Ser176GlnfsTer9
NM_153758.5:c.526del MANE Select	NP_715639.2:p.Ser176GlnfsTer9