Canonical Allele Identifier: CA1657315302

Gene: RSPH4A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.116617527_116617529delinsTCC , CM000668.2:g.116617527_116617529delinsTCC	GRCh38
NC_000006.11:g.116938690_116938692delinsTCC , CM000668.1:g.116938690_116938692delinsTCC	GRCh37
NC_000006.10:g.117045383_117045385delinsTCC	NCBI36
NG_012934.1:g.6049_6051delinsTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229554.10:c.686+218_686+220delinsTCC MANE Select	ENSP00000229554.5:n.686+218_686+220delinsTCC
ENST00000229554.9:c.686+218_686+220delinsTCC	ENSP00000229554.5:n.686+218_686+220delinsTCC
ENST00000368580.4:c.686+218_686+220delinsTCC	ENSP00000357569.4:n.686+218_686+220delinsTCC
ENST00000368581.8:c.686+218_686+220delinsTCC	ENSP00000357570.4:n.686+218_686+220delinsTCC
NM_001010892.2:c.686+218_686+220delinsTCC	NP_001010892.1:n.686+218_686+220delinsTCC
NM_001161664.1:c.686+218_686+220delinsTCC	NP_001155136.1:n.686+218_686+220delinsTCC
XM_006715469.2:c.686+218_686+220delinsTCC	XP_006715532.1:n.686+218_686+220delinsTCC
XM_011535791.1:c.686+218_686+220delinsTCC	XP_011534093.1:n.686+218_686+220delinsTCC
XM_011535792.1:c.686+218_686+220delinsTCC	XP_011534094.1:n.686+218_686+220delinsTCC
XR_942416.1:n.3337+218_3337+220delinsTCC
XM_017010826.1:c.686+218_686+220delinsTCC	XP_016866315.1:n.686+218_686+220delinsTCC
NM_001010892.3:c.686+218_686+220delinsTCC MANE Select	NP_001010892.1:n.686+218_686+220delinsTCC
NM_001161664.2:c.686+218_686+220delinsTCC	NP_001155136.1:n.686+218_686+220delinsTCC