Canonical Allele Identifier: CA407022694

Gene: KLK3

Linked Data

• gnomAD v4: 19-50858244-T-C
• MyVariant Identifiers: chr19:g.51361500T>C (hg19) ; chr19:g.50858244T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858244T>C , CM000681.2:g.50858244T>C	GRCh38
NC_000019.9:g.51361500T>C , CM000681.1:g.51361500T>C	GRCh37
NC_000019.8:g.56053312T>C	NCBI36
NG_011653.1:g.8330T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.422T>C MANE Select	ENSP00000314151.1:p.Leu141Pro
ENST00000326003.6:c.422T>C	ENSP00000314151.1:p.Leu141Pro
ENST00000360617.7:c.422T>C	ENSP00000353829.2:p.Leu141Pro
ENST00000422986.6:c.*78T>C	ENSP00000393628.2:n.*78T>C
ENST00000593997.5:c.422T>C	ENSP00000472907.1:p.Leu141Pro
ENST00000595392.5:c.353-55T>C	ENSP00000468912.1:n.353-55T>C
ENST00000595952.5:c.293T>C	ENSP00000471155.1:p.Leu98Pro
ENST00000596185.5:c.*530T>C	ENSP00000471648.1:n.*530T>C
ENST00000596333.1:n.457T>C
ENST00000597286.5:c.311T>C	ENSP00000470523.1:p.Leu104Pro
ENST00000597483.5:c.293T>C	ENSP00000472411.1:p.Leu98Pro
ENST00000598145.1:c.406T>C
ENST00000601349.5:n.1701T>C
ENST00000601503.5:c.365T>C	ENSP00000472213.1:p.Leu122Pro
ENST00000601812.1:n.854T>C
ENST00000617027.4:c.354-55T>C	ENSP00000483513.1:n.354-55T>C
NM_001030047.1:c.422T>C	NP_001025218.1:p.Leu141Pro
NM_001030048.1:c.293T>C	NP_001025219.1:p.Leu98Pro
NM_001648.2:c.422T>C MANE Select	NP_001639.1:p.Leu141Pro
XM_011526923.1:c.422T>C	XP_011525225.1:p.Leu141Pro
XM_011526924.1:c.422T>C	XP_011525226.1:p.Leu141Pro
XR_935817.1:n.457T>C