Canonical Allele Identifier: CA2586639263

Gene: KLK3

Linked Data

• gnomAD v4: 19-50860148-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860148T>G , CM000681.2:g.50860148T>G	GRCh38
NC_000019.9:g.51363404T>G , CM000681.1:g.51363404T>G	GRCh37
NC_000019.8:g.56055216T>G	NCBI36
NG_011653.1:g.10234T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000326003.7:c.*21T>G MANE Select	ENSP00000314151.1:n.*21T>G
ENST00000326003.6:c.*21T>G	ENSP00000314151.1:n.*21T>G
ENST00000360617.7:c.1249T>G	ENSP00000353829.2:n.1249T>G
ENST00000422986.6:c.*463T>G	ENSP00000393628.2:n.*463T>G
ENST00000595392.5:c.*308T>G	ENSP00000468912.1:n.*308T>G
ENST00000595952.5:c.*21T>G	ENSP00000471155.1:n.*21T>G
ENST00000596333.1:n.985T>G
ENST00000598145.1:c.809T>G
ENST00000601349.5:n.2086T>G
ENST00000617027.4:c.*21T>G	ENSP00000483513.1:n.*21T>G
NM_001030047.1:c.*532T>G	NP_001025218.1:n.*532T>G
NM_001030048.1:c.*21T>G	NP_001025219.1:n.*21T>G
NM_001648.2:c.*21T>G MANE Select	NP_001639.1:n.*21T>G
XM_011526923.1:c.*21T>G	XP_011525225.1:n.*21T>G
XR_935817.1:n.1324+894T>G