Canonical Allele Identifier: CA9604576

Gene: KLK3

Linked Data

• dbSNP Id: rs759946194
• ExAC: 19:51363203 A / C
• gnomAD v2: 19-51363203-A-C
• gnomAD v3: 19-50859947-A-C
• gnomAD v4: 19-50859947-A-C
• MyVariant Identifiers: chr19:g.51363203A>C (hg19) ; chr19:g.50859947A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50859947A>C , CM000681.2:g.50859947A>C	GRCh38
NC_000019.9:g.51363203A>C , CM000681.1:g.51363203A>C	GRCh37
NC_000019.8:g.56055015A>C	NCBI36
NG_011653.1:g.10033A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.631-25A>C MANE Select	ENSP00000314151.1:n.631-25A>C
ENST00000326003.6:c.631-25A>C	ENSP00000314151.1:n.631-25A>C
ENST00000360617.7:c.1048A>C	ENSP00000353829.2:n.1048A>C
ENST00000422986.6:c.*287-25A>C	ENSP00000393628.2:n.*287-25A>C
ENST00000595392.5:c.*132-25A>C	ENSP00000468912.1:n.*132-25A>C
ENST00000595952.5:c.502-25A>C	ENSP00000471155.1:n.502-25A>C
ENST00000596185.5:c.*739-25A>C	ENSP00000471648.1:n.*739-25A>C
ENST00000596333.1:n.809-25A>C
ENST00000598145.1:c.633-25A>C
ENST00000601349.5:n.1910-25A>C
ENST00000601812.1:n.1063-25A>C
ENST00000617027.4:c.508-25A>C	ENSP00000483513.1:n.508-25A>C
NM_001030047.1:c.*331A>C	NP_001025218.1:n.*331A>C
NM_001030048.1:c.502-25A>C	NP_001025219.1:n.502-25A>C
NM_001648.2:c.631-25A>C MANE Select	NP_001639.1:n.631-25A>C
XM_011526923.1:c.649-25A>C	XP_011525225.1:n.649-25A>C
XM_011526924.1:c.*331A>C	XP_011525226.1:n.*331A>C
XR_935817.1:n.1324+693A>C