Canonical Allele Identifier: CA2814740545

Gene: KLK3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50859863_50859864insGATAGGATGGGGTGTCTGTGTTATTTGTG , CM000681.2:g.50859863_50859864insGATAGGATGGGGTGTCTGTGTTATTTGTG	GRCh38
NC_000019.9:g.51363119_51363120insGATAGGATGGGGTGTCTGTGTTATTTGTG , CM000681.1:g.51363119_51363120insGATAGGATGGGGTGTCTGTGTTATTTGTG	GRCh37
NC_000019.8:g.56054931_56054932insGATAGGATGGGGTGTCTGTGTTATTTGTG	NCBI36
NG_011653.1:g.9949_9950insGATAGGATGGGGTGTCTGTGTTATTTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.631-109_631-108insGATAGGATGGGGTGTCTGTGTTATTTGTG MANE Select	ENSP00000314151.1:n.631-109_631-108insGATAGGATGGGGTGTCTGTGTTA...
ENST00000326003.6:c.631-109_631-108insGATAGGATGGGGTGTCTGTGTTATTTGTG	ENSP00000314151.1:n.631-109_631-108insGATAGGATGGGGTGTCTGTGTTA...
ENST00000360617.7:c.964_965insGATAGGATGGGGTGTCTGTGTTATTTGTG	ENSP00000353829.2:n.964_965insGATAGGATGGGGTGTCTGTGTTATTTGTG
ENST00000422986.6:c.*287-109_*287-108insGATAGGATGGGGTGTCTGTGTTATTTGTG	ENSP00000393628.2:n.*287-109_*287-108insGATAGGATGGGGTGTCTGTGT...
ENST00000595392.5:c.*132-109_*132-108insGATAGGATGGGGTGTCTGTGTTATTTGTG	ENSP00000468912.1:n.*132-109_*132-108insGATAGGATGGGGTGTCTGTGT...
ENST00000595952.5:c.502-109_502-108insGATAGGATGGGGTGTCTGTGTTATTTGTG	ENSP00000471155.1:n.502-109_502-108insGATAGGATGGGGTGTCTGTGTTA...
ENST00000596185.5:c.*739-109_*739-108insGATAGGATGGGGTGTCTGTGTTATTTGTG	ENSP00000471648.1:n.*739-109_*739-108insGATAGGATGGGGTGTCTGTGT...
ENST00000596333.1:n.809-109_809-108insGATAGGATGGGGTGTCTGTGTTATTTGTG
ENST00000598145.1:c.633-109_633-108insGATAGGATGGGGTGTCTGTGTTATTTGTG
ENST00000601349.5:n.1910-109_1910-108insGATAGGATGGGGTGTCTGTGTTATTTGTG
ENST00000601812.1:n.1063-109_1063-108insGATAGGATGGGGTGTCTGTGTTATTTGTG
ENST00000617027.4:c.508-109_508-108insGATAGGATGGGGTGTCTGTGTTATTTGTG	ENSP00000483513.1:n.508-109_508-108insGATAGGATGGGGTGTCTGTGTTA...
NM_001030047.1:c.*247_*248insGATAGGATGGGGTGTCTGTGTTATTTGTG	NP_001025218.1:n.*247_*248insGATAGGATGGGGTGTCTGTGTTATTTGTG
NM_001030048.1:c.502-109_502-108insGATAGGATGGGGTGTCTGTGTTATTTGTG	NP_001025219.1:n.502-109_502-108insGATAGGATGGGGTGTCTGTGTTATTT...
NM_001648.2:c.631-109_631-108insGATAGGATGGGGTGTCTGTGTTATTTGTG MANE Select	NP_001639.1:n.631-109_631-108insGATAGGATGGGGTGTCTGTGTTATTTGTG...
XM_011526923.1:c.649-109_649-108insGATAGGATGGGGTGTCTGTGTTATTTGTG	XP_011525225.1:n.649-109_649-108insGATAGGATGGGGTGTCTGTGTTATTT...
XM_011526924.1:c.*247_*248insGATAGGATGGGGTGTCTGTGTTATTTGTG	XP_011525226.1:n.*247_*248insGATAGGATGGGGTGTCTGTGTTATTTGTG
XR_935817.1:n.1324+609_1324+610insGATAGGATGGGGTGTCTGTGTTATTTGTG