Canonical Allele Identifier: CA2576867207

Gene: KLK3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858347C>G , CM000681.2:g.50858347C>G	GRCh38
NC_000019.9:g.51361603C>G , CM000681.1:g.51361603C>G	GRCh37
NC_000019.8:g.56053415C>G	NCBI36
NG_011653.1:g.8433C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.493+32C>G MANE Select	ENSP00000314151.1:n.493+32C>G
ENST00000326003.6:c.493+32C>G	ENSP00000314151.1:n.493+32C>G
ENST00000360617.7:c.493+32C>G	ENSP00000353829.2:n.493+32C>G
ENST00000422986.6:c.*149+32C>G	ENSP00000393628.2:n.*149+32C>G
ENST00000593997.5:c.493+32C>G	ENSP00000472907.1:n.493+32C>G
ENST00000595392.5:c.369+32C>G	ENSP00000468912.1:n.369+32C>G
ENST00000595952.5:c.364+32C>G	ENSP00000471155.1:n.364+32C>G
ENST00000596185.5:c.*601+32C>G	ENSP00000471648.1:n.*601+32C>G
ENST00000596333.1:n.560C>G
ENST00000597286.5:c.382+32C>G	ENSP00000470523.1:n.382+32C>G
ENST00000597483.5:c.364+32C>G	ENSP00000472411.1:n.364+32C>G
ENST00000598145.1:c.495+14C>G
ENST00000601349.5:n.1772+32C>G
ENST00000601503.5:c.436+32C>G	ENSP00000472213.1:n.436+32C>G
ENST00000601812.1:n.925+32C>G
ENST00000617027.4:c.370+32C>G	ENSP00000483513.1:n.370+32C>G
NM_001030047.1:c.493+32C>G	NP_001025218.1:n.493+32C>G
NM_001030048.1:c.364+32C>G	NP_001025219.1:n.364+32C>G
NM_001648.2:c.493+32C>G MANE Select	NP_001639.1:n.493+32C>G
XM_011526923.1:c.511+14C>G	XP_011525225.1:n.511+14C>G
XM_011526924.1:c.511+14C>G	XP_011525226.1:n.511+14C>G
XR_935817.1:n.528+32C>G