Canonical Allele Identifier: CA1909611760

Gene: PRKG1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.51482829C= , CM000672.2:g.51482829C=	GRCh38
NC_000010.10:g.53242589C= , CM000672.1:g.53242589C=	GRCh37
NC_000010.9:g.52912595C=	NCBI36
NG_029982.1:g.496679C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373976.9:c.592+14993C=	ENSP00000363087.4:n.592+14993C=
ENST00000373980.11:c.592+14993C= MANE Select	ENSP00000363092.5:n.592+14993C=
ENST00000401604.8:c.547+14993C=	ENSP00000384200.4:n.547+14993C=
ENST00000643582.1:c.592+14993C=	ENSP00000495279.1:n.592+14993C=
ENST00000643704.1:c.592+14993C=	ENSP00000496551.1:n.592+14993C=
ENST00000645324.1:c.592+14993C=	ENSP00000494124.1:n.592+14993C=
ENST00000645790.1:n.114+14993C=
ENST00000373976.8:c.166+14993C=	ENSP00000363087.3:n.166+14993C=
ENST00000373980.8:c.592+14993C=	ENSP00000363092.4:n.592+14993C=
ENST00000373985.5:c.547+14993C=	ENSP00000363097.2:n.547+14993C=
NM_001098512.2:c.547+14993C=	NP_001091982.1:n.547+14993C=
NM_006258.3:c.592+14993C=	NP_006249.1:n.592+14993C=
XM_011539952.1:c.592+14993C=	XP_011538254.1:n.592+14993C=
NM_001098512.3:c.547+14993C=	NP_001091982.1:n.547+14993C=
NM_006258.4:c.592+14993C= MANE Select	NP_006249.1:n.592+14993C=
XM_011539952.2:c.592+14993C=	XP_011538254.1:n.592+14993C=
XM_017016412.1:c.307+14993C=	XP_016871901.1:n.307+14993C=
XM_017016413.1:c.289+14993C=	XP_016871902.1:n.289+14993C=
NM_001374782.1:c.592+14993C=	NP_001361711.1:n.592+14993C=