Canonical Allele Identifier: CA707488624

Gene: PRKCH

Linked Data

• dbSNP Id: rs1432853746
• MyVariant Identifiers: chr14:g.61908362_61908363del (hg19) ; chr14:g.61441644_61441645del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.61441647_61441648del , CM000676.2:g.61441647_61441648del	GRCh38
NC_000014.8:g.61908365_61908366del , CM000676.1:g.61908365_61908366del	GRCh37
NC_000014.7:g.60978118_60978119del	NCBI36
NG_011514.1:g.124851_124852del

Transcript Alleles

HGVS	Amino-acid change
ENST00000332981.11:c.428-1464_428-1463del MANE Select	ENSP00000329127.5:n.428-1464_428-1463del
ENST00000332981.10:c.428-1464_428-1463del	ENSP00000329127.5:n.428-1464_428-1463del
ENST00000332981.9:c.428-1464_428-1463del	ENSP00000329127.5:n.428-1464_428-1463del
ENST00000553265.5:c.-56-1464_-56-1463del	ENSP00000451933.1:n.-56-1464_-56-1463del
ENST00000553726.5:c.-229-4045_-229-4044del	ENSP00000451793.1:n.-229-4045_-229-4044de...
ENST00000553830.1:c.254-1464_254-1463del	ENSP00000452588.1:n.254-1464_254-1463del
ENST00000553831.5:c.-56-1464_-56-1463del	ENSP00000450959.1:n.-56-1464_-56-1463del
ENST00000555082.5:c.-56-1464_-56-1463del	ENSP00000450981.1:n.-56-1464_-56-1463del
ENST00000555185.5:c.-18-43855_-18-43854del	ENSP00000451871.1:n.-18-43855_-18-43854de...
ENST00000555542.5:c.-56-1464_-56-1463del	ENSP00000451789.1:n.-56-1464_-56-1463del
ENST00000555906.5:c.-56-1464_-56-1463del	ENSP00000451205.1:n.-56-1464_-56-1463del
ENST00000556164.5:c.-56-1464_-56-1463del	ENSP00000452330.1:n.-56-1464_-56-1463del
ENST00000556778.5:c.-56-1464_-56-1463del	ENSP00000452055.1:n.-56-1464_-56-1463del
ENST00000557585.5:c.-56-1464_-56-1463del	ENSP00000451930.1:n.-56-1464_-56-1463del
NM_006255.4:c.428-1464_428-1463del	NP_006246.2:n.428-1464_428-1463del
XM_011536954.1:c.191-1464_191-1463del	XP_011535256.1:n.191-1464_191-1463del
XM_011536955.1:c.188-1464_188-1463del	XP_011535257.1:n.188-1464_188-1463del
XM_011536956.1:c.428-1464_428-1463del	XP_011535258.1:n.428-1464_428-1463del
XM_011536957.1:c.428-1464_428-1463del	XP_011535259.1:n.428-1464_428-1463del
XM_011536954.3:c.191-1464_191-1463del	XP_011535256.1:n.191-1464_191-1463del
XM_017021458.1:c.-56-1464_-56-1463del	XP_016876947.1:n.-56-1464_-56-1463del
XM_017021459.1:c.428-1464_428-1463del	XP_016876948.1:n.428-1464_428-1463del
XM_024449661.1:c.-56-1464_-56-1463del	XP_024305429.1:n.-56-1464_-56-1463del
XM_024449662.1:c.-56-1464_-56-1463del	XP_024305430.1:n.-56-1464_-56-1463del
NM_006255.5:c.428-1464_428-1463del MANE Select	NP_006246.2:n.428-1464_428-1463del