Canonical Allele Identifier: CA2341115638

Gene: KLK3

Linked Data

• dbSNP Id: rs1599997061
• gnomAD v4: 19-50860191-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860191A>C , CM000681.2:g.50860191A>C	GRCh38
NC_000019.9:g.51363447A>C , CM000681.1:g.51363447A>C	GRCh37
NC_000019.8:g.56055259A>C	NCBI36
NG_011653.1:g.10277A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.*64A>C MANE Select	ENSP00000314151.1:n.*64A>C
ENST00000326003.6:c.*64A>C	ENSP00000314151.1:n.*64A>C
ENST00000360617.7:c.1292A>C	ENSP00000353829.2:n.1292A>C
ENST00000422986.6:c.*506A>C	ENSP00000393628.2:n.*506A>C
ENST00000595392.5:c.*351A>C	ENSP00000468912.1:n.*351A>C
ENST00000595952.5:c.*64A>C	ENSP00000471155.1:n.*64A>C
ENST00000596333.1:n.1028A>C
ENST00000598145.1:c.852A>C
ENST00000601349.5:n.2129A>C
ENST00000617027.4:c.*64A>C	ENSP00000483513.1:n.*64A>C
NM_001030047.1:c.*575A>C	NP_001025218.1:n.*575A>C
NM_001030048.1:c.*64A>C	NP_001025219.1:n.*64A>C
NM_001648.2:c.*64A>C MANE Select	NP_001639.1:n.*64A>C
XM_011526923.1:c.*64A>C	XP_011525225.1:n.*64A>C
XR_935817.1:n.1324+937A>C