Canonical Allele Identifier: CA5503802

Gene: PRKG1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.52271475C>T , CM000672.2:g.52271475C>T	GRCh38
NC_000010.10:g.54031235C>T , CM000672.1:g.54031235C>T	GRCh37
NC_000010.9:g.53701241C>T	NCBI36
NG_029982.1:g.1285325C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373975.3:n.658C>T
ENST00000373980.11:c.1299C>T MANE Select	ENSP00000363092.5:p.Ser433=
ENST00000401604.8:c.1254C>T	ENSP00000384200.4:p.Ser418=
ENST00000672084.1:c.450C>T	ENSP00000499822.1:p.Ser150=
ENST00000373975.2:n.748C>T
ENST00000373980.8:c.1299C>T	ENSP00000363092.4:p.Ser433=
ENST00000373985.5:c.1254C>T	ENSP00000363097.2:p.Ser418=
ENST00000401604.6:c.618C>T	ENSP00000384200.3:p.Ser206=
NM_001098512.2:c.1254C>T	NP_001091982.1:p.Ser418=
NM_006258.3:c.1299C>T	NP_006249.1:p.Ser433=
XM_005269972.3:c.450C>T	XP_005270029.1:p.Ser150=
NM_001098512.3:c.1254C>T	NP_001091982.1:p.Ser418=
NM_006258.4:c.1299C>T MANE Select	NP_006249.1:p.Ser433=
XM_017016412.1:c.1014C>T	XP_016871901.1:p.Ser338=
XM_017016413.1:c.996C>T	XP_016871902.1:p.Ser332=
XM_024448078.1:c.90C>T	XP_024303846.1:p.Ser30=
NM_001374781.1:c.90C>T	NP_001361710.1:p.Ser30=