Canonical Allele Identifier: CA1657315020
Gene: RSPH4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.116617289_116617290delinsCA , CM000668.2:g.116617289_116617290delinsCA GRCh38
NC_000006.11:g.116938452_116938453delinsCA , CM000668.1:g.116938452_116938453delinsCA GRCh37
NC_000006.10:g.117045145_117045146delinsCA NCBI36
NG_012934.1:g.5811_5812delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000229554.10:c.666_667delinsCA MANE Select ENSP00000229554.5:p.Ser222=
ENST00000229554.9:c.666_667delinsCA ENSP00000229554.5:p.Ser222=
ENST00000368580.4:c.666_667delinsCA ENSP00000357569.4:p.Ser222=
ENST00000368581.8:c.666_667delinsCA ENSP00000357570.4:p.Ser222=
NM_001010892.2:c.666_667delinsCA NP_001010892.1:p.Ser222=
NM_001161664.1:c.666_667delinsCA NP_001155136.1:p.Ser222=
XM_006715469.2:c.666_667delinsCA XP_006715532.1:p.Ser222=
XM_011535791.1:c.666_667delinsCA XP_011534093.1:p.Ser222=
XM_011535792.1:c.666_667delinsCA XP_011534094.1:p.Ser222=
XR_942416.1:n.3317_3318delinsCA
XM_017010826.1:c.666_667delinsCA XP_016866315.1:p.Ser222=
NM_001010892.3:c.666_667delinsCA MANE Select NP_001010892.1:p.Ser222=
NM_001161664.2:c.666_667delinsCA NP_001155136.1:p.Ser222=