Canonical Allele Identifier: CA2394917452
Gene: IL17RA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.17085254_17085255delinsAG , CM000684.2:g.17085254_17085255delinsAG GRCh38
NC_000022.10:g.17566144_17566145delinsAG , CM000684.1:g.17566144_17566145delinsAG GRCh37
NC_000022.9:g.15946144_15946145delinsAG NCBI36
NG_028257.1:g.5294_5295delinsAG , LRG_355:g.5294_5295delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000612619.2:c.138+25_138+26delinsAG ENSP00000479970.1:n.138+25_138+26delinsAG
ENST00000694948.1:n.236+25_236+26delinsAG
ENST00000694949.1:n.233+25_233+26delinsAG
ENST00000694950.1:c.218+25_218+26delinsAG
ENST00000319363.11:c.138+25_138+26delinsAG MANE Select ENSP00000320936.6:n.138+25_138+26delinsAG
ENST00000319363.10:c.138+25_138+26delinsAG ENSP00000320936.6:n.138+25_138+26delinsAG
ENST00000459971.1:n.173+25_173+26delinsAG
ENST00000477874.1:n.276+25_276+26delinsAG
ENST00000612619.1:c.138+25_138+26delinsAG ENSP00000479970.1:n.138+25_138+26delinsAG
NM_001289905.1:c.138+25_138+26delinsAG NP_001276834.1:n.138+25_138+26delinsAG
NM_014339.6:c.138+25_138+26delinsAG , LRG_355t1:c.138+25_138+26delinsAG NP_055154.3:n.138+25_138+26delinsAG
NM_014339.7:c.138+25_138+26delinsAG MANE Select NP_055154.3:n.138+25_138+26delinsAG
NM_001289905.2:c.138+25_138+26delinsAG NP_001276834.1:n.138+25_138+26delinsAG