Canonical Allele Identifier: CA2772741013

Gene: RSPH4A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.116617551_116617552insTTTT , CM000668.2:g.116617551_116617552insTTTT	GRCh38
NC_000006.11:g.116938714_116938715insTTTT , CM000668.1:g.116938714_116938715insTTTT	GRCh37
NC_000006.10:g.117045407_117045408insTTTT	NCBI36
NG_012934.1:g.6073_6074insTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229554.10:c.686+242_686+243insTTTT MANE Select	ENSP00000229554.5:n.686+242_686+243insTTTT
ENST00000229554.9:c.686+242_686+243insTTTT	ENSP00000229554.5:n.686+242_686+243insTTTT
ENST00000368580.4:c.686+242_686+243insTTTT	ENSP00000357569.4:n.686+242_686+243insTTTT
ENST00000368581.8:c.686+242_686+243insTTTT	ENSP00000357570.4:n.686+242_686+243insTTTT
NM_001010892.2:c.686+242_686+243insTTTT	NP_001010892.1:n.686+242_686+243insTTTT
NM_001161664.1:c.686+242_686+243insTTTT	NP_001155136.1:n.686+242_686+243insTTTT
XM_006715469.2:c.686+242_686+243insTTTT	XP_006715532.1:n.686+242_686+243insTTTT
XM_011535791.1:c.686+242_686+243insTTTT	XP_011534093.1:n.686+242_686+243insTTTT
XM_011535792.1:c.686+242_686+243insTTTT	XP_011534094.1:n.686+242_686+243insTTTT
XR_942416.1:n.3337+242_3337+243insTTTT
XM_017010826.1:c.686+242_686+243insTTTT	XP_016866315.1:n.686+242_686+243insTTTT
NM_001010892.3:c.686+242_686+243insTTTT MANE Select	NP_001010892.1:n.686+242_686+243insTTTT
NM_001161664.2:c.686+242_686+243insTTTT	NP_001155136.1:n.686+242_686+243insTTTT