Canonical Allele Identifier: CA407025237

Gene: KLK3

Linked Data

• gnomAD v4: 19-50860114-T-C
• MyVariant Identifiers: chr19:g.51363370T>C (hg19) ; chr19:g.50860114T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860114T>C , CM000681.2:g.50860114T>C	GRCh38
NC_000019.9:g.51363370T>C , CM000681.1:g.51363370T>C	GRCh37
NC_000019.8:g.56055182T>C	NCBI36
NG_011653.1:g.10200T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.773T>C MANE Select	ENSP00000314151.1:p.Val258Ala
ENST00000326003.6:c.773T>C	ENSP00000314151.1:p.Val258Ala
ENST00000360617.7:c.1215T>C	ENSP00000353829.2:n.1215T>C
ENST00000422986.6:c.*429T>C	ENSP00000393628.2:n.*429T>C
ENST00000595392.5:c.*274T>C	ENSP00000468912.1:n.*274T>C
ENST00000595952.5:c.644T>C	ENSP00000471155.1:p.Val215Ala
ENST00000596333.1:n.951T>C
ENST00000598145.1:c.775T>C
ENST00000601349.5:n.2052T>C
ENST00000601812.1:n.1205T>C
ENST00000617027.4:c.650T>C	ENSP00000483513.1:p.Val217Ala
NM_001030047.1:c.*498T>C	NP_001025218.1:n.*498T>C
NM_001030048.1:c.644T>C	NP_001025219.1:p.Val215Ala
NM_001648.2:c.773T>C MANE Select	NP_001639.1:p.Val258Ala
XM_011526923.1:c.791T>C	XP_011525225.1:p.Val264Ala
XR_935817.1:n.1324+860T>C