Canonical Allele Identifier: CA3970864
Gene: RSPH4A HGNC NCBI

Linked Data

dbSNP Id: rs781003909

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.116627605del , CM000668.2:g.116627605del GRCh38
NC_000006.11:g.116948768del , CM000668.1:g.116948768del GRCh37
NC_000006.10:g.117055461del NCBI36
NG_012934.1:g.16127del

Transcript Alleles

HGVS Amino-acid Change
ENST00000229554.10:c.922-24del MANE Select ENSP00000229554.5:n.922-24del
ENST00000229554.9:c.922-24del ENSP00000229554.5:n.922-24del
ENST00000368580.4:c.922-1962del ENSP00000357569.4:n.922-1962del
ENST00000368581.8:c.922-24del ENSP00000357570.4:n.922-24del
NM_001010892.2:c.922-24del NP_001010892.1:n.922-24del
NM_001161664.1:c.922-24del NP_001155136.1:n.922-24del
XM_006715469.2:c.922-24del XP_006715532.1:n.922-24del
XM_011535791.1:c.922-24del XP_011534093.1:n.922-24del
XM_011535792.1:c.922-24del XP_011534094.1:n.922-24del
XR_942416.1:n.3573-24del
XM_017010826.1:c.922-24del XP_016866315.1:n.922-24del
NM_001010892.3:c.922-24del MANE Select NP_001010892.1:n.922-24del
NM_001161664.2:c.922-24del NP_001155136.1:n.922-24del