Canonical Allele Identifier: CA2341115605

Gene: KLK3

Linked Data

• dbSNP Id: rs2090176051
• gnomAD v4: 19-50860133-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860133C>T , CM000681.2:g.50860133C>T	GRCh38
NC_000019.9:g.51363389C>T , CM000681.1:g.51363389C>T	GRCh37
NC_000019.8:g.56055201C>T	NCBI36
NG_011653.1:g.10219C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.*6C>T MANE Select	ENSP00000314151.1:n.*6C>T
ENST00000326003.6:c.*6C>T	ENSP00000314151.1:n.*6C>T
ENST00000360617.7:c.1234C>T	ENSP00000353829.2:n.1234C>T
ENST00000422986.6:c.*448C>T	ENSP00000393628.2:n.*448C>T
ENST00000595392.5:c.*293C>T	ENSP00000468912.1:n.*293C>T
ENST00000595952.5:c.*6C>T	ENSP00000471155.1:n.*6C>T
ENST00000596333.1:n.970C>T
ENST00000598145.1:c.794C>T
ENST00000601349.5:n.2071C>T
ENST00000617027.4:c.*6C>T	ENSP00000483513.1:n.*6C>T
NM_001030047.1:c.*517C>T	NP_001025218.1:n.*517C>T
NM_001030048.1:c.*6C>T	NP_001025219.1:n.*6C>T
NM_001648.2:c.*6C>T MANE Select	NP_001639.1:n.*6C>T
XM_011526923.1:c.*6C>T	XP_011525225.1:n.*6C>T
XR_935817.1:n.1324+879C>T