Canonical Allele Identifier: CA1909586895

Gene: PRKG1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.51311193T>G , CM000672.2:g.51311193T>G	GRCh38
NC_000010.10:g.53070953T>G , CM000672.1:g.53070953T>G	GRCh37
NC_000010.9:g.52740959T>G	NCBI36
NG_029982.1:g.325043T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373976.9:c.479-156530T>G	ENSP00000363087.4:n.479-156530T>G
ENST00000373980.11:c.479-156530T>G MANE Select	ENSP00000363092.5:n.479-156530T>G
ENST00000401604.8:c.434-156530T>G	ENSP00000384200.4:n.434-156530T>G
ENST00000643582.1:c.479-156530T>G	ENSP00000495279.1:n.479-156530T>G
ENST00000643704.1:c.479-156530T>G	ENSP00000496551.1:n.479-156530T>G
ENST00000645324.1:c.479-156530T>G	ENSP00000494124.1:n.479-156530T>G
ENST00000373976.8:c.53-156530T>G	ENSP00000363087.3:n.53-156530T>G
ENST00000373980.8:c.479-156530T>G	ENSP00000363092.4:n.479-156530T>G
ENST00000373985.5:c.434-156530T>G	ENSP00000363097.2:n.434-156530T>G
NM_001098512.2:c.434-156530T>G	NP_001091982.1:n.434-156530T>G
NM_006258.3:c.479-156530T>G	NP_006249.1:n.479-156530T>G
XM_011539952.1:c.479-156530T>G	XP_011538254.1:n.479-156530T>G
NM_001098512.3:c.434-156530T>G	NP_001091982.1:n.434-156530T>G
NM_006258.4:c.479-156530T>G MANE Select	NP_006249.1:n.479-156530T>G
XM_011539952.2:c.479-156530T>G	XP_011538254.1:n.479-156530T>G
XM_017016412.1:c.194-156530T>G	XP_016871901.1:n.194-156530T>G
XM_017016413.1:c.176-156530T>G	XP_016871902.1:n.176-156530T>G
NM_001374782.1:c.479-156530T>G	NP_001361711.1:n.479-156530T>G