Canonical Allele Identifier: CA1657309687

Gene: RSPH4A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.116627700_116627703delinsAGAT , CM000668.2:g.116627700_116627703delinsAGAT	GRCh38
NC_000006.11:g.116948863_116948866delinsAGAT , CM000668.1:g.116948863_116948866delinsAGAT	GRCh37
NC_000006.10:g.117055556_117055559delinsAGAT	NCBI36
NG_012934.1:g.16222_16225delinsAGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229554.10:c.993_996delinsAGAT MANE Select	ENSP00000229554.5:p.Thr331=
ENST00000229554.9:c.993_996delinsAGAT	ENSP00000229554.5:p.Thr331=
ENST00000368580.4:c.922-1867_922-1864delinsAGAT	ENSP00000357569.4:n.922-1867_922-1864delinsAGAT
ENST00000368581.8:c.993_996delinsAGAT	ENSP00000357570.4:p.Thr331=
NM_001010892.2:c.993_996delinsAGAT	NP_001010892.1:p.Thr331=
NM_001161664.1:c.993_996delinsAGAT	NP_001155136.1:p.Thr331=
XM_006715469.2:c.993_996delinsAGAT	XP_006715532.1:p.Thr331=
XM_011535791.1:c.993_996delinsAGAT	XP_011534093.1:p.Thr331=
XM_011535792.1:c.993_996delinsAGAT	XP_011534094.1:p.Thr331=
XR_942416.1:n.3644_3647delinsAGAT
XM_017010826.1:c.993_996delinsAGAT	XP_016866315.1:p.Thr331=
NM_001010892.3:c.993_996delinsAGAT MANE Select	NP_001010892.1:p.Thr331=
NM_001161664.2:c.993_996delinsAGAT	NP_001155136.1:p.Thr331=