Canonical Allele Identifier: CA883221738

Gene: KLK3

Linked Data

• dbSNP Id: rs1405514971
• gnomAD v3: 19-50859831-G-A
• gnomAD v4: 19-50859831-G-A
• MyVariant Identifiers: chr19:g.51363087G>A (hg19) ; chr19:g.50859831G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50859831G>A , CM000681.2:g.50859831G>A	GRCh38
NC_000019.9:g.51363087G>A , CM000681.1:g.51363087G>A	GRCh37
NC_000019.8:g.56054899G>A	NCBI36
NG_011653.1:g.9917G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.631-141G>A MANE Select	ENSP00000314151.1:n.631-141G>A
ENST00000326003.6:c.631-141G>A	ENSP00000314151.1:n.631-141G>A
ENST00000360617.7:c.932G>A	ENSP00000353829.2:n.932G>A
ENST00000422986.6:c.*287-141G>A	ENSP00000393628.2:n.*287-141G>A
ENST00000595392.5:c.*132-141G>A	ENSP00000468912.1:n.*132-141G>A
ENST00000595952.5:c.502-141G>A	ENSP00000471155.1:n.502-141G>A
ENST00000596185.5:c.*739-141G>A	ENSP00000471648.1:n.*739-141G>A
ENST00000596333.1:n.809-141G>A
ENST00000598145.1:c.633-141G>A
ENST00000601349.5:n.1910-141G>A
ENST00000601812.1:n.1063-141G>A
ENST00000617027.4:c.508-141G>A	ENSP00000483513.1:n.508-141G>A
NM_001030047.1:c.*215G>A	NP_001025218.1:n.*215G>A
NM_001030048.1:c.502-141G>A	NP_001025219.1:n.502-141G>A
NM_001648.2:c.631-141G>A MANE Select	NP_001639.1:n.631-141G>A
XM_011526923.1:c.649-141G>A	XP_011525225.1:n.649-141G>A
XM_011526924.1:c.*215G>A	XP_011525226.1:n.*215G>A
XR_935817.1:n.1324+577G>A