Canonical Allele Identifier: CA2341114677
Gene: KLK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50858404G= , CM000681.2:g.50858404G= GRCh38
NC_000019.9:g.51361660G= , CM000681.1:g.51361660G= GRCh37
NC_000019.8:g.56053472G= NCBI36
NG_011653.1:g.8490G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.494-55G= MANE Select ENSP00000314151.1:n.494-55G=
ENST00000326003.6:c.494-55G= ENSP00000314151.1:n.494-55G=
ENST00000360617.7:c.494-55G= ENSP00000353829.2:n.494-55G=
ENST00000422986.6:c.*150-55G= ENSP00000393628.2:n.*150-55G=
ENST00000593997.5:c.494-55G= ENSP00000472907.1:n.494-55G=
ENST00000595392.5:c.370-55G= ENSP00000468912.1:n.370-55G=
ENST00000595952.5:c.365-55G= ENSP00000471155.1:n.365-55G=
ENST00000596185.5:c.*602-55G= ENSP00000471648.1:n.*602-55G=
ENST00000596333.1:n.617G=
ENST00000597286.5:c.383-55G= ENSP00000470523.1:n.383-55G=
ENST00000597483.5:c.365-55G= ENSP00000472411.1:n.365-55G=
ENST00000598145.1:c.496-55G=
ENST00000601349.5:n.1773-55G=
ENST00000601503.5:c.437-55G= ENSP00000472213.1:n.437-55G=
ENST00000601812.1:n.926-55G=
ENST00000617027.4:c.371-55G= ENSP00000483513.1:n.371-55G=
NM_001030047.1:c.494-55G= NP_001025218.1:n.494-55G=
NM_001030048.1:c.365-55G= NP_001025219.1:n.365-55G=
NM_001648.2:c.494-55G= MANE Select NP_001639.1:n.494-55G=
XM_011526923.1:c.512-55G= XP_011525225.1:n.512-55G=
XM_011526924.1:c.512-55G= XP_011525226.1:n.512-55G=
XR_935817.1:n.529-55G=