Canonical Allele Identifier: CA2586637932

Gene: KLK3

Linked Data

• gnomAD v4: 19-50858387-T-TGGGTCTG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858387_50858388insGGGTCTG , CM000681.2:g.50858387_50858388insGGGTCTG	GRCh38
NC_000019.9:g.51361643_51361644insGGGTCTG , CM000681.1:g.51361643_51361644insGGGTCTG	GRCh37
NC_000019.8:g.56053455_56053456insGGGTCTG	NCBI36
NG_011653.1:g.8473_8474insGGGTCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.494-72_494-71insGGGTCTG MANE Select	ENSP00000314151.1:n.494-72_494-71insGGGTCTG
ENST00000326003.6:c.494-72_494-71insGGGTCTG	ENSP00000314151.1:n.494-72_494-71insGGGTCTG
ENST00000360617.7:c.494-72_494-71insGGGTCTG	ENSP00000353829.2:n.494-72_494-71insGGGTCTG
ENST00000422986.6:c.*150-72_*150-71insGGGTCTG	ENSP00000393628.2:n.*150-72_*150-71insGGGTCTG
ENST00000593997.5:c.494-72_494-71insGGGTCTG	ENSP00000472907.1:n.494-72_494-71insGGGTCTG
ENST00000595392.5:c.370-72_370-71insGGGTCTG	ENSP00000468912.1:n.370-72_370-71insGGGTCTG
ENST00000595952.5:c.365-72_365-71insGGGTCTG	ENSP00000471155.1:n.365-72_365-71insGGGTCTG
ENST00000596185.5:c.*602-72_*602-71insGGGTCTG	ENSP00000471648.1:n.*602-72_*602-71insGGGTCTG
ENST00000596333.1:n.600_601insGGGTCTG
ENST00000597286.5:c.383-72_383-71insGGGTCTG	ENSP00000470523.1:n.383-72_383-71insGGGTCTG
ENST00000597483.5:c.365-72_365-71insGGGTCTG	ENSP00000472411.1:n.365-72_365-71insGGGTCTG
ENST00000598145.1:c.495+54_495+55insGGGTCTG
ENST00000601349.5:n.1773-72_1773-71insGGGTCTG
ENST00000601503.5:c.437-72_437-71insGGGTCTG	ENSP00000472213.1:n.437-72_437-71insGGGTCTG
ENST00000601812.1:n.926-72_926-71insGGGTCTG
ENST00000617027.4:c.371-72_371-71insGGGTCTG	ENSP00000483513.1:n.371-72_371-71insGGGTCTG
NM_001030047.1:c.494-72_494-71insGGGTCTG	NP_001025218.1:n.494-72_494-71insGGGTCTG
NM_001030048.1:c.365-72_365-71insGGGTCTG	NP_001025219.1:n.365-72_365-71insGGGTCTG
NM_001648.2:c.494-72_494-71insGGGTCTG MANE Select	NP_001639.1:n.494-72_494-71insGGGTCTG
XM_011526923.1:c.511+54_511+55insGGGTCTG	XP_011525225.1:n.511+54_511+55insGGGTCTG
XM_011526924.1:c.511+54_511+55insGGGTCTG	XP_011525226.1:n.511+54_511+55insGGGTCTG
XR_935817.1:n.529-72_529-71insGGGTCTG