Canonical Allele Identifier: CA505749925

Gene: PRKCSH

Linked Data

• MyVariant Identifiers: chr19:g.11558286C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11447471C>G , CM000681.2:g.11447471C>G	GRCh38
NC_000019.9:g.11558286C>G , CM000681.1:g.11558286C>G	GRCh37
NC_000019.8:g.11419286C>G	NCBI36
NG_009300.1:g.17018C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000591462.6:c.882C>G	ENSP00000465489.1:p.Ala294=
ENST00000677123.1:c.882C>G MANE Select	ENSP00000503163.1:p.Ala294=
ENST00000585325.5:n.155C>G
ENST00000585540.1:n.73C>G
ENST00000587327.5:c.882C>G	ENSP00000466012.1:p.Ala294=
ENST00000589838.5:c.882C>G	ENSP00000465461.1:p.Ala294=
ENST00000591462.5:c.882C>G	ENSP00000465489.1:p.Ala294=
ENST00000592445.1:n.129C>G
ENST00000592741.5:c.882C>G	ENSP00000466134.1:p.Ala294=
NM_001001329.2:c.882C>G	NP_001001329.1:p.Ala294=
NM_001289102.1:c.882C>G	NP_001276031.1:p.Ala294=
NM_001289103.1:c.882C>G	NP_001276032.1:p.Ala294=
NM_001289104.1:c.882C>G	NP_001276033.1:p.Ala294=
NM_002743.3:c.882C>G	NP_002734.2:p.Ala294=
XM_011528130.1:c.882C>G	XP_011526432.1:p.Ala294=
XM_011528131.1:c.882C>G	XP_011526433.1:p.Ala294=
XM_011528132.1:c.882C>G	XP_011526434.1:p.Ala294=
XM_017026977.2:c.882C>G	XP_016882466.1:p.Ala294=
XM_024451602.1:c.882C>G	XP_024307370.1:p.Ala294=
NM_001001329.3:c.882C>G	NP_001001329.1:p.Ala294=
NM_001289102.2:c.882C>G	NP_001276031.1:p.Ala294=
NM_001289103.2:c.882C>G	NP_001276032.1:p.Ala294=
NM_001289104.2:c.882C>G MANE Select	NP_001276033.1:p.Ala294=
NM_001379608.1:c.882C>G	NP_001366537.1:p.Ala294=
NM_001379609.1:c.882C>G	NP_001366538.1:p.Ala294=