Canonical Allele Identifier: CA5503660

Gene: PRKG1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.52062602A>C , CM000672.2:g.52062602A>C	GRCh38
NC_000010.10:g.53822362A>C , CM000672.1:g.53822362A>C	GRCh37
NC_000010.9:g.53492368A>C	NCBI36
NG_029982.1:g.1076452A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373975.3:n.204A>C
ENST00000373976.9:c.906A>C	ENSP00000363087.4:p.Gly302=
ENST00000373980.11:c.906A>C MANE Select	ENSP00000363092.5:p.Gly302=
ENST00000401604.8:c.861A>C	ENSP00000384200.4:p.Gly287=
ENST00000645324.1:c.906A>C	ENSP00000494124.1:p.Gly302=
ENST00000646354.1:n.323A>C
ENST00000373975.2:n.294A>C
ENST00000373976.8:c.480A>C	ENSP00000363087.3:p.Gly160=
ENST00000373980.8:c.906A>C	ENSP00000363092.4:p.Gly302=
ENST00000373985.5:c.861A>C	ENSP00000363097.2:p.Gly287=
ENST00000401604.6:c.225A>C	ENSP00000384200.3:p.Gly75=
NM_001098512.2:c.861A>C	NP_001091982.1:p.Gly287=
NM_006258.3:c.906A>C	NP_006249.1:p.Gly302=
XM_011539952.1:c.906A>C	XP_011538254.1:p.Gly302=
NM_001098512.3:c.861A>C	NP_001091982.1:p.Gly287=
NM_006258.4:c.906A>C MANE Select	NP_006249.1:p.Gly302=
XM_011539952.2:c.906A>C	XP_011538254.1:p.Gly302=
XM_017016412.1:c.621A>C	XP_016871901.1:p.Gly207=
XM_017016413.1:c.603A>C	XP_016871902.1:p.Gly201=
XM_024448078.1:c.-304A>C	XP_024303846.1:n.-304A>C
NM_001374781.1:c.-304A>C	NP_001361710.1:n.-304A>C
NM_001374782.1:c.906A>C	NP_001361711.1:p.Gly302=