Canonical Allele Identifier: CA2341115642

Gene: KLK3

Linked Data

• dbSNP Id: rs2090176757
• gnomAD v4: 19-50860197-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860197C>A , CM000681.2:g.50860197C>A	GRCh38
NC_000019.9:g.51363453C>A , CM000681.1:g.51363453C>A	GRCh37
NC_000019.8:g.56055265C>A	NCBI36
NG_011653.1:g.10283C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.*70C>A MANE Select	ENSP00000314151.1:n.*70C>A
ENST00000326003.6:c.*70C>A	ENSP00000314151.1:n.*70C>A
ENST00000360617.7:c.1298C>A	ENSP00000353829.2:n.1298C>A
ENST00000422986.6:c.*512C>A	ENSP00000393628.2:n.*512C>A
ENST00000595392.5:c.*357C>A	ENSP00000468912.1:n.*357C>A
ENST00000595952.5:c.*70C>A	ENSP00000471155.1:n.*70C>A
ENST00000596333.1:n.1034C>A
ENST00000598145.1:c.858C>A
ENST00000601349.5:n.2135C>A
ENST00000617027.4:c.*70C>A	ENSP00000483513.1:n.*70C>A
NM_001030047.1:c.*581C>A	NP_001025218.1:n.*581C>A
NM_001030048.1:c.*70C>A	NP_001025219.1:n.*70C>A
NM_001648.2:c.*70C>A MANE Select	NP_001639.1:n.*70C>A
XM_011526923.1:c.*70C>A	XP_011525225.1:n.*70C>A
XR_935817.1:n.1324+943C>A