Canonical Allele Identifier: CA2586638982

Gene: KLK3

Linked Data

• gnomAD v4: 19-50860226-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860226T>G , CM000681.2:g.50860226T>G	GRCh38
NC_000019.9:g.51363482T>G , CM000681.1:g.51363482T>G	GRCh37
NC_000019.8:g.56055294T>G	NCBI36
NG_011653.1:g.10312T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.*99T>G MANE Select	ENSP00000314151.1:n.*99T>G
ENST00000326003.6:c.*99T>G	ENSP00000314151.1:n.*99T>G
ENST00000360617.7:c.1327T>G	ENSP00000353829.2:n.1327T>G
ENST00000422986.6:c.*541T>G	ENSP00000393628.2:n.*541T>G
ENST00000595392.5:c.*386T>G	ENSP00000468912.1:n.*386T>G
ENST00000595952.5:c.*99T>G	ENSP00000471155.1:n.*99T>G
ENST00000596333.1:n.1063T>G
ENST00000601349.5:n.2164T>G
ENST00000617027.4:c.*99T>G	ENSP00000483513.1:n.*99T>G
NM_001030047.1:c.*610T>G	NP_001025218.1:n.*610T>G
NM_001030048.1:c.*99T>G	NP_001025219.1:n.*99T>G
NM_001648.2:c.*99T>G MANE Select	NP_001639.1:n.*99T>G
XM_011526923.1:c.*99T>G	XP_011525225.1:n.*99T>G
XR_935817.1:n.1324+972T>G