Canonical Allele Identifier: CA2813609352

Gene: PRKCSH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11449179_11449268del , CM000681.2:g.11449179_11449268del	GRCh38
NC_000019.9:g.11559994_11560083del , CM000681.1:g.11559994_11560083del	GRCh37
NC_000019.8:g.11420994_11421083del	NCBI36
NG_009300.1:g.18726_18815del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000591462.6:c.1431+4_1434del
ENST00000677123.1:c.1461+4_1464del
ENST00000586486.1:c.456+4_459del
ENST00000587290.5:n.623+4_626del
ENST00000587327.5:c.1431+4_1434del
ENST00000589838.5:c.1440+4_1443del
ENST00000591462.5:c.1431+4_1434del
ENST00000592435.1:n.355+4_358del
ENST00000592741.5:c.1461+4_1464del
NM_001001329.2:c.1431+4_1434del
NM_001289102.1:c.1431+4_1434del
NM_001289103.1:c.1461+4_1464del
NM_001289104.1:c.1461+4_1464del
NM_002743.3:c.1440+4_1443del
XM_011528130.1:c.1461+4_1464del
XM_011528131.1:c.1440+4_1443del
XM_011528132.1:c.1431+4_1434del
XM_017026977.2:c.1440+4_1443del
XM_024451602.1:c.1431+4_1434del
NM_001001329.3:c.1431+4_1434del
NM_001289102.2:c.1431+4_1434del
NM_001289103.2:c.1461+4_1464del
NM_001289104.2:c.1461+4_1464del
NM_001379608.1:c.1440+4_1443del
NM_001379609.1:c.1431+4_1434del