Canonical Allele Identifier: CA2581361199
Gene: KLK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50860192A>C , CM000681.2:g.50860192A>C GRCh38
NC_000019.9:g.51363448A>C , CM000681.1:g.51363448A>C GRCh37
NC_000019.8:g.56055260A>C NCBI36
NG_011653.1:g.10278A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.*65A>C MANE Select ENSP00000314151.1:n.*65A>C
ENST00000326003.6:c.*65A>C ENSP00000314151.1:n.*65A>C
ENST00000360617.7:c.1293A>C ENSP00000353829.2:n.1293A>C
ENST00000422986.6:c.*507A>C ENSP00000393628.2:n.*507A>C
ENST00000595392.5:c.*352A>C ENSP00000468912.1:n.*352A>C
ENST00000595952.5:c.*65A>C ENSP00000471155.1:n.*65A>C
ENST00000596333.1:n.1029A>C
ENST00000598145.1:c.853A>C
ENST00000601349.5:n.2130A>C
ENST00000617027.4:c.*65A>C ENSP00000483513.1:n.*65A>C
NM_001030047.1:c.*576A>C NP_001025218.1:n.*576A>C
NM_001030048.1:c.*65A>C NP_001025219.1:n.*65A>C
NM_001648.2:c.*65A>C MANE Select NP_001639.1:n.*65A>C
XM_011526923.1:c.*65A>C XP_011525225.1:n.*65A>C
XR_935817.1:n.1324+938A>C