Canonical Allele Identifier: CA883221759

Gene: KLK3

Linked Data

• dbSNP Id: rs1267252433
• gnomAD v3: 19-50859865-G-T
• gnomAD v4: 19-50859865-G-T
• MyVariant Identifiers: chr19:g.51363121G>T (hg19) ; chr19:g.50859865G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50859865G>T , CM000681.2:g.50859865G>T	GRCh38
NC_000019.9:g.51363121G>T , CM000681.1:g.51363121G>T	GRCh37
NC_000019.8:g.56054933G>T	NCBI36
NG_011653.1:g.9951G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.631-107G>T MANE Select	ENSP00000314151.1:n.631-107G>T
ENST00000326003.6:c.631-107G>T	ENSP00000314151.1:n.631-107G>T
ENST00000360617.7:c.966G>T	ENSP00000353829.2:n.966G>T
ENST00000422986.6:c.*287-107G>T	ENSP00000393628.2:n.*287-107G>T
ENST00000595392.5:c.*132-107G>T	ENSP00000468912.1:n.*132-107G>T
ENST00000595952.5:c.502-107G>T	ENSP00000471155.1:n.502-107G>T
ENST00000596185.5:c.*739-107G>T	ENSP00000471648.1:n.*739-107G>T
ENST00000596333.1:n.809-107G>T
ENST00000598145.1:c.633-107G>T
ENST00000601349.5:n.1910-107G>T
ENST00000601812.1:n.1063-107G>T
ENST00000617027.4:c.508-107G>T	ENSP00000483513.1:n.508-107G>T
NM_001030047.1:c.*249G>T	NP_001025218.1:n.*249G>T
NM_001030048.1:c.502-107G>T	NP_001025219.1:n.502-107G>T
NM_001648.2:c.631-107G>T MANE Select	NP_001639.1:n.631-107G>T
XM_011526923.1:c.649-107G>T	XP_011525225.1:n.649-107G>T
XM_011526924.1:c.*249G>T	XP_011525226.1:n.*249G>T
XR_935817.1:n.1324+611G>T