Canonical Allele Identifier: CA2341115665

Gene: KLK3

Linked Data

• dbSNP Id: rs1309375900
• gnomAD v4: 19-50860238-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860238G>T , CM000681.2:g.50860238G>T	GRCh38
NC_000019.9:g.51363494G>T , CM000681.1:g.51363494G>T	GRCh37
NC_000019.8:g.56055306G>T	NCBI36
NG_011653.1:g.10324G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.*111G>T MANE Select	ENSP00000314151.1:n.*111G>T
ENST00000326003.6:c.*111G>T	ENSP00000314151.1:n.*111G>T
ENST00000360617.7:c.1339G>T	ENSP00000353829.2:n.1339G>T
ENST00000422986.6:c.*553G>T	ENSP00000393628.2:n.*553G>T
ENST00000595392.5:c.*398G>T	ENSP00000468912.1:n.*398G>T
ENST00000595952.5:c.*111G>T	ENSP00000471155.1:n.*111G>T
ENST00000596333.1:n.1075G>T
ENST00000601349.5:n.2176G>T
ENST00000617027.4:c.*111G>T	ENSP00000483513.1:n.*111G>T
NM_001030047.1:c.*622G>T	NP_001025218.1:n.*622G>T
NM_001030048.1:c.*111G>T	NP_001025219.1:n.*111G>T
NM_001648.2:c.*111G>T MANE Select	NP_001639.1:n.*111G>T
XM_011526923.1:c.*111G>T	XP_011525225.1:n.*111G>T
XR_935817.1:n.1324+984G>T