Canonical Allele Identifier: CA309633845

Gene: KLK3

Linked Data

• dbSNP Id: rs1047122140
• gnomAD v2: 19-51363208-C-T
• gnomAD v4: 19-50859952-C-T
• MyVariant Identifiers: chr19:g.51363208C>T (hg19) ; chr19:g.50859952C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50859952C>T , CM000681.2:g.50859952C>T	GRCh38
NC_000019.9:g.51363208C>T , CM000681.1:g.51363208C>T	GRCh37
NC_000019.8:g.56055020C>T	NCBI36
NG_011653.1:g.10038C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.631-20C>T MANE Select	ENSP00000314151.1:n.631-20C>T
ENST00000326003.6:c.631-20C>T	ENSP00000314151.1:n.631-20C>T
ENST00000360617.7:c.1053C>T	ENSP00000353829.2:n.1053C>T
ENST00000422986.6:c.*287-20C>T	ENSP00000393628.2:n.*287-20C>T
ENST00000595392.5:c.*132-20C>T	ENSP00000468912.1:n.*132-20C>T
ENST00000595952.5:c.502-20C>T	ENSP00000471155.1:n.502-20C>T
ENST00000596185.5:c.*739-20C>T	ENSP00000471648.1:n.*739-20C>T
ENST00000596333.1:n.809-20C>T
ENST00000598145.1:c.633-20C>T
ENST00000601349.5:n.1910-20C>T
ENST00000601812.1:n.1063-20C>T
ENST00000617027.4:c.508-20C>T	ENSP00000483513.1:n.508-20C>T
NM_001030047.1:c.*336C>T	NP_001025218.1:n.*336C>T
NM_001030048.1:c.502-20C>T	NP_001025219.1:n.502-20C>T
NM_001648.2:c.631-20C>T MANE Select	NP_001639.1:n.631-20C>T
XM_011526923.1:c.649-20C>T	XP_011525225.1:n.649-20C>T
XM_011526924.1:c.*336C>T	XP_011525226.1:n.*336C>T
XR_935817.1:n.1324+698C>T