Canonical Allele Identifier: CA2771056900
Gene: IL17A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186477_52186478del , CM000668.2:g.52186477_52186478del GRCh38
NC_000006.11:g.52051275_52051276del , CM000668.1:g.52051275_52051276del GRCh37
NC_000006.10:g.52159234_52159235del NCBI36
NG_033021.1:g.5091_5092del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.27+19_27+20del MANE Select ENSP00000497968.1:n.27+19_27+20del
ENST00000340057.1:c.27+19_27+20del ENSP00000344192.1:n.27+19_27+20del
NM_002190.2:c.27+19_27+20del NP_002181.1:n.27+19_27+20del
NM_002190.3:c.27+19_27+20del MANE Select NP_002181.1:n.27+19_27+20del
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