Canonical Allele Identifier: CA2586638998

Gene: KLK3

Linked Data

• gnomAD v4: 19-50860241-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860241T>G , CM000681.2:g.50860241T>G	GRCh38
NC_000019.9:g.51363497T>G , CM000681.1:g.51363497T>G	GRCh37
NC_000019.8:g.56055309T>G	NCBI36
NG_011653.1:g.10327T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.*114T>G MANE Select	ENSP00000314151.1:n.*114T>G
ENST00000326003.6:c.*114T>G	ENSP00000314151.1:n.*114T>G
ENST00000360617.7:c.1342T>G	ENSP00000353829.2:n.1342T>G
ENST00000422986.6:c.*556T>G	ENSP00000393628.2:n.*556T>G
ENST00000595392.5:c.*401T>G	ENSP00000468912.1:n.*401T>G
ENST00000595952.5:c.*114T>G	ENSP00000471155.1:n.*114T>G
ENST00000596333.1:n.1078T>G
ENST00000601349.5:n.2179T>G
ENST00000617027.4:c.*114T>G	ENSP00000483513.1:n.*114T>G
NM_001030047.1:c.*625T>G	NP_001025218.1:n.*625T>G
NM_001030048.1:c.*114T>G	NP_001025219.1:n.*114T>G
NM_001648.2:c.*114T>G MANE Select	NP_001639.1:n.*114T>G
XM_011526923.1:c.*114T>G	XP_011525225.1:n.*114T>G
XR_935817.1:n.1324+987T>G