Canonical Allele Identifier: CA1089007511
Gene: IL17A HGNC NCBI

Linked Data

dbSNP Id: rs1763285909

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186443del , CM000668.2:g.52186443del GRCh38
NC_000006.11:g.52051241del , CM000668.1:g.52051241del GRCh37
NC_000006.10:g.52159200del NCBI36
NG_033021.1:g.5057del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.12del MANE Select ENSP00000497968.1:p.Lys5ArgfsTer11
ENST00000340057.1:c.12del ENSP00000344192.1:p.Lys5ArgfsTer11
NM_002190.2:c.12del NP_002181.1:p.Lys5ArgfsTer11
NM_002190.3:c.12del MANE Select NP_002181.1:p.Lys5ArgfsTer11