Canonical Allele Identifier: CA2679089666
Gene: IL17A HGNC NCBI

Linked Data

gnomAD v4: 6-52186471-C-CCTG
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186471_52186472insCTG , CM000668.2:g.52186471_52186472insCTG GRCh38
NC_000006.11:g.52051269_52051270insCTG , CM000668.1:g.52051269_52051270insCTG GRCh37
NC_000006.10:g.52159228_52159229insCTG NCBI36
NG_033021.1:g.5085_5086insCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.27+13_27+14insCTG MANE Select ENSP00000497968.1:n.27+13_27+14insCTG
ENST00000340057.1:c.27+13_27+14insCTG ENSP00000344192.1:n.27+13_27+14insCTG
NM_002190.2:c.27+13_27+14insCTG NP_002181.1:n.27+13_27+14insCTG
NM_002190.3:c.27+13_27+14insCTG MANE Select NP_002181.1:n.27+13_27+14insCTG
Search 100 bp 5'
Search 100 bp 3'