Canonical Allele Identifier: CA2650221024
Gene: IL19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206842615_206842637del , CM000663.2:g.206842615_206842637del GRCh38
NC_000001.10:g.207015960_207015982del , CM000663.1:g.207015960_207015982del GRCh37
NC_000001.9:g.205082583_205082605del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000659997.3:c.527_*15del MANE Select ENSP00000499459.2:n.[c.527_*15del;Ser176TyrfsTer?]
ENST00000340758.7:c.527_*15del ENSP00000343000.3:n.[c.527_*15del;Ser176TyrfsTer?]
ENST00000656872.2:c.527_*15del ENSP00000499487.2:n.[c.527_*15del;Ser176TyrfsTer?]
ENST00000659997.2:c.527_*15del ENSP00000499459.2:n.[c.527_*15del;Ser176TyrfsTer?]
ENST00000340758.6:c.641_*15del ENSP00000343000.2:n.[c.641_*15del;Ser214TyrfsTer?]
ENST00000620365.1:c.527_*15del ENSP00000482668.1:n.[c.527_*15del;Ser176TyrfsTer?]
NM_013371.3:c.527_*15del NP_037503.2:n.[c.527_*15del;Ser176TyrfsTer?]
NM_153758.2:c.641_*15del NP_715639.1:n.[c.641_*15del;Ser214TyrfsTer?]
XR_922482.1:n.186_208del
XR_922482.2:n.186_208del
NM_001369605.1:c.527_*15del NP_001356534.1:n.[c.527_*15del;Ser176TyrfsTer?]
NM_153758.3:c.641_*15del NP_715639.1:n.[c.641_*15del;Ser214TyrfsTer?]
NM_001393490.1:c.527_*15del NP_001380419.1:n.[c.527_*15del;Ser176TyrfsTer?]
NM_001393491.1:c.527_*15del NP_001380420.1:n.[c.527_*15del;Ser176TyrfsTer?]
NM_013371.5:c.527_*15del NP_037503.2:n.[c.527_*15del;Ser176TyrfsTer?]
NM_153758.5:c.527_*15del MANE Select NP_715639.2:n.[c.527_*15del;Ser176TyrfsTer?]