Canonical Allele Identifier: CA1909898732

Gene: PRKG1

Linked Data

• dbSNP Id: rs1903989

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.52010479C>T , CM000672.2:g.52010479C>T	GRCh38
NC_000010.10:g.53770239C>T , CM000672.1:g.53770239C>T	GRCh37
NC_000010.9:g.53440245C>T	NCBI36
NG_029982.1:g.1024329C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000373976.9:c.763-44005C>T	ENSP00000363087.4:n.763-44005C>T
ENST00000373980.11:c.763-44005C>T MANE Select	ENSP00000363092.5:n.763-44005C>T
ENST00000401604.8:c.718-44005C>T	ENSP00000384200.4:n.718-44005C>T
ENST00000645324.1:c.763-44005C>T	ENSP00000494124.1:n.763-44005C>T
ENST00000373976.8:c.337-44005C>T	ENSP00000363087.3:n.337-44005C>T
ENST00000373980.8:c.763-44005C>T	ENSP00000363092.4:n.763-44005C>T
ENST00000373985.5:c.718-44005C>T	ENSP00000363097.2:n.718-44005C>T
ENST00000401604.6:c.82-44005C>T	ENSP00000384200.3:n.82-44005C>T
NM_001098512.2:c.718-44005C>T	NP_001091982.1:n.718-44005C>T
NM_006258.3:c.763-44005C>T	NP_006249.1:n.763-44005C>T
XM_011539952.1:c.763-44005C>T	XP_011538254.1:n.763-44005C>T
NM_001098512.3:c.718-44005C>T	NP_001091982.1:n.718-44005C>T
NM_006258.4:c.763-44005C>T MANE Select	NP_006249.1:n.763-44005C>T
XM_011539952.2:c.763-44005C>T	XP_011538254.1:n.763-44005C>T
XM_017016412.1:c.478-44005C>T	XP_016871901.1:n.478-44005C>T
XM_017016413.1:c.460-44005C>T	XP_016871902.1:n.460-44005C>T
NM_001374782.1:c.763-44005C>T	NP_001361711.1:n.763-44005C>T