Canonical Allele Identifier: CA2586639269

Gene: KLK3

Linked Data

• gnomAD v4: 19-50860159-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860159T>A , CM000681.2:g.50860159T>A	GRCh38
NC_000019.9:g.51363415T>A , CM000681.1:g.51363415T>A	GRCh37
NC_000019.8:g.56055227T>A	NCBI36
NG_011653.1:g.10245T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000326003.7:c.*32T>A MANE Select	ENSP00000314151.1:n.*32T>A
ENST00000326003.6:c.*32T>A	ENSP00000314151.1:n.*32T>A
ENST00000360617.7:c.1260T>A	ENSP00000353829.2:n.1260T>A
ENST00000422986.6:c.*474T>A	ENSP00000393628.2:n.*474T>A
ENST00000595392.5:c.*319T>A	ENSP00000468912.1:n.*319T>A
ENST00000595952.5:c.*32T>A	ENSP00000471155.1:n.*32T>A
ENST00000596333.1:n.996T>A
ENST00000598145.1:c.820T>A
ENST00000601349.5:n.2097T>A
ENST00000617027.4:c.*32T>A	ENSP00000483513.1:n.*32T>A
NM_001030047.1:c.*543T>A	NP_001025218.1:n.*543T>A
NM_001030048.1:c.*32T>A	NP_001025219.1:n.*32T>A
NM_001648.2:c.*32T>A MANE Select	NP_001639.1:n.*32T>A
XM_011526923.1:c.*32T>A	XP_011525225.1:n.*32T>A
XR_935817.1:n.1324+905T>A