Canonical Allele Identifier: CA2582533985

Gene: PRKCSH

Linked Data

• gnomAD v4: 19-11447152-CGGTCCGAGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11447153_11447161del , CM000681.2:g.11447153_11447161del	GRCh38
NC_000019.9:g.11557968_11557976del , CM000681.1:g.11557968_11557976del	GRCh37
NC_000019.8:g.11418968_11418976del	NCBI36
NG_009300.1:g.16700_16708del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000591462.6:c.842_849+1del
ENST00000677123.1:c.842_849+1del
ENST00000585325.5:n.115_122+1del
ENST00000585540.1:n.33_40+1del
ENST00000587327.5:c.842_849+1del
ENST00000589838.5:c.842_849+1del
ENST00000591462.5:c.842_849+1del
ENST00000592445.1:n.89_96+1del
ENST00000592741.5:c.842_849+1del
NM_001001329.2:c.842_849+1del
NM_001289102.1:c.842_849+1del
NM_001289103.1:c.842_849+1del
NM_001289104.1:c.842_849+1del
NM_002743.3:c.842_849+1del
XM_011528130.1:c.842_849+1del
XM_011528131.1:c.842_849+1del
XM_011528132.1:c.842_849+1del
XM_017026977.2:c.842_849+1del
XM_024451602.1:c.842_849+1del
NM_001001329.3:c.842_849+1del
NM_001289102.2:c.842_849+1del
NM_001289103.2:c.842_849+1del
NM_001289104.2:c.842_849+1del
NM_001379608.1:c.842_849+1del
NM_001379609.1:c.842_849+1del