Canonical Allele Identifier: CA1603651609

Gene: GRK6

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177437201T= , CM000667.2:g.177437201T=	GRCh38
NC_000005.9:g.176864202T= , CM000667.1:g.176864202T=	GRCh37
NC_000005.8:g.176796808T=	NCBI36
NG_031981.1:g.15516T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001004106.3:c.1404+671T= MANE Select	NP_001004106.1:n.1404+671T=
ENST00000355472.10:c.1404+671T= MANE Select	ENSP00000347655.5:n.1404+671T=
NM_001004105.2:c.1404+671T=	NP_001004105.1:n.1404+671T=
NM_001004105.3:c.1404+671T=	NP_001004105.1:n.1404+671T=
NM_001004106.2:c.1404+671T=	NP_001004106.1:n.1404+671T=
NM_001364164.1:c.774+671T=	NP_001351093.1:n.774+671T=
NM_001364164.2:c.774+671T=	NP_001351093.1:n.774+671T=
NM_002082.3:c.1404+671T=	NP_002073.2:n.1404+671T=
NM_002082.4:c.1404+671T=	NP_002073.2:n.1404+671T=
ENST00000355472.9:c.1404+671T=	ENSP00000347655.5:n.1404+671T=
ENST00000355958.9:c.1404+671T=	ENSP00000348230.5:n.1404+671T=
ENST00000393576.7:c.1302+671T=	ENSP00000377204.3:n.1302+671T=
ENST00000515666.5:n.1540+671T=
ENST00000528793.5:c.1404+671T=	ENSP00000433511.1:n.1404+671T=
XM_006714858.2:c.1314+671T=	XP_006714921.1:n.1314+671T=
XM_006714858.3:c.1314+671T=	XP_006714921.1:n.1314+671T=
XM_006714859.2:c.1308+671T=	XP_006714922.1:n.1308+671T=
XM_011534537.1:c.1287+671T=	XP_011532839.1:n.1287+671T=
XM_011534537.2:c.1287+671T=	XP_011532839.1:n.1287+671T=
XM_011534538.1:c.609+671T=	XP_011532840.1:n.609+671T=
XM_024446032.1:c.774+671T=	XP_024301800.1:n.774+671T=