Canonical Allele Identifier: CA407022482
Gene: KLK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50858180G>C , CM000681.2:g.50858180G>C GRCh38
NC_000019.9:g.51361436G>C , CM000681.1:g.51361436G>C GRCh37
NC_000019.8:g.56053248G>C NCBI36
NG_011653.1:g.8266G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.358G>C MANE Select ENSP00000314151.1:p.Asp120His
ENST00000326003.6:c.358G>C ENSP00000314151.1:p.Asp120His
ENST00000360617.7:c.358G>C ENSP00000353829.2:p.Asp120His
ENST00000422986.6:c.*14G>C ENSP00000393628.2:n.*14G>C
ENST00000593997.5:c.358G>C ENSP00000472907.1:p.Asp120His
ENST00000595392.5:c.352+6G>C ENSP00000468912.1:n.352+6G>C
ENST00000595952.5:c.229G>C ENSP00000471155.1:p.Asp77His
ENST00000596185.5:c.*466G>C ENSP00000471648.1:n.*466G>C
ENST00000596333.1:n.393G>C
ENST00000597286.5:c.247G>C ENSP00000470523.1:p.Asp83His
ENST00000597483.5:c.229G>C ENSP00000472411.1:p.Asp77His
ENST00000598145.1:c.342G>C
ENST00000601349.5:n.1637G>C
ENST00000601503.5:c.301G>C ENSP00000472213.1:p.Asp101His
ENST00000601812.1:n.790G>C
ENST00000617027.4:c.353+5G>C ENSP00000483513.1:n.353+5G>C
NM_001030047.1:c.358G>C NP_001025218.1:p.Asp120His
NM_001030048.1:c.229G>C NP_001025219.1:p.Asp77His
NM_001648.2:c.358G>C MANE Select NP_001639.1:p.Asp120His
XM_011526923.1:c.358G>C XP_011525225.1:p.Asp120His
XM_011526924.1:c.358G>C XP_011525226.1:p.Asp120His
XR_935817.1:n.393G>C