Canonical Allele Identifier: CA2341115449
Gene: KLK3 HGNC NCBI

Linked Data

dbSNP Id: rs1599996282

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50859802T>C , CM000681.2:g.50859802T>C GRCh38
NC_000019.9:g.51363058T>C , CM000681.1:g.51363058T>C GRCh37
NC_000019.8:g.56054870T>C NCBI36
NG_011653.1:g.9888T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.631-170T>C MANE Select ENSP00000314151.1:n.631-170T>C
ENST00000326003.6:c.631-170T>C ENSP00000314151.1:n.631-170T>C
ENST00000360617.7:c.903T>C ENSP00000353829.2:n.903T>C
ENST00000422986.6:c.*287-170T>C ENSP00000393628.2:n.*287-170T>C
ENST00000595392.5:c.*132-170T>C ENSP00000468912.1:n.*132-170T>C
ENST00000595952.5:c.502-170T>C ENSP00000471155.1:n.502-170T>C
ENST00000596185.5:c.*739-170T>C ENSP00000471648.1:n.*739-170T>C
ENST00000596333.1:n.809-170T>C
ENST00000597483.5:c.*186T>C ENSP00000472411.1:n.*186T>C
ENST00000598145.1:c.633-170T>C
ENST00000601349.5:n.1910-170T>C
ENST00000601812.1:n.1063-170T>C
ENST00000617027.4:c.508-170T>C ENSP00000483513.1:n.508-170T>C
NM_001030047.1:c.*186T>C NP_001025218.1:n.*186T>C
NM_001030048.1:c.502-170T>C NP_001025219.1:n.502-170T>C
NM_001648.2:c.631-170T>C MANE Select NP_001639.1:n.631-170T>C
XM_011526923.1:c.649-170T>C XP_011525225.1:n.649-170T>C
XM_011526924.1:c.*186T>C XP_011525226.1:n.*186T>C
XR_935817.1:n.1324+548T>C