Canonical Allele Identifier: CA1657309646

Gene: RSPH4A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.116627669A= , CM000668.2:g.116627669A=	GRCh38
NC_000006.11:g.116948832A= , CM000668.1:g.116948832A=	GRCh37
NC_000006.10:g.117055525A=	NCBI36
NG_012934.1:g.16191A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229554.10:c.962A= MANE Select	ENSP00000229554.5:p.Tyr321=
ENST00000229554.9:c.962A=	ENSP00000229554.5:p.Tyr321=
ENST00000368580.4:c.922-1898A=	ENSP00000357569.4:n.922-1898A=
ENST00000368581.8:c.962A=	ENSP00000357570.4:p.Tyr321=
NM_001010892.2:c.962A=	NP_001010892.1:p.Tyr321=
NM_001161664.1:c.962A=	NP_001155136.1:p.Tyr321=
XM_006715469.2:c.962A=	XP_006715532.1:p.Tyr321=
XM_011535791.1:c.962A=	XP_011534093.1:p.Tyr321=
XM_011535792.1:c.962A=	XP_011534094.1:p.Tyr321=
XR_942416.1:n.3613A=
XM_017010826.1:c.962A=	XP_016866315.1:p.Tyr321=
NM_001010892.3:c.962A= MANE Select	NP_001010892.1:p.Tyr321=
NM_001161664.2:c.962A=	NP_001155136.1:p.Tyr321=