Canonical Allele Identifier: CA1657314570

Gene: RSPH4A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.116616948C= , CM000668.2:g.116616948C=	GRCh38
NC_000006.11:g.116938111C= , CM000668.1:g.116938111C=	GRCh37
NC_000006.10:g.117044804C=	NCBI36
NG_012934.1:g.5470C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000229554.10:c.325C= MANE Select	ENSP00000229554.5:p.Gln109=
ENST00000229554.9:c.325C=	ENSP00000229554.5:p.Gln109=
ENST00000368580.4:c.325C=	ENSP00000357569.4:p.Gln109=
ENST00000368581.8:c.325C=	ENSP00000357570.4:p.Gln109=
NM_001010892.2:c.325C=	NP_001010892.1:p.Gln109=
NM_001161664.1:c.325C=	NP_001155136.1:p.Gln109=
XM_006715469.2:c.325C=	XP_006715532.1:p.Gln109=
XM_011535791.1:c.325C=	XP_011534093.1:p.Gln109=
XM_011535792.1:c.325C=	XP_011534094.1:p.Gln109=
XR_942416.1:n.2976C=
XM_017010826.1:c.325C=	XP_016866315.1:p.Gln109=
NM_001010892.3:c.325C= MANE Select	NP_001010892.1:p.Gln109=
NM_001161664.2:c.325C=	NP_001155136.1:p.Gln109=