Canonical Allele Identifier: CA407022751

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51361521T>A (hg19) ; chr19:g.50858265T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858265T>A , CM000681.2:g.50858265T>A	GRCh38
NC_000019.9:g.51361521T>A , CM000681.1:g.51361521T>A	GRCh37
NC_000019.8:g.56053333T>A	NCBI36
NG_011653.1:g.8351T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.443T>A MANE Select	ENSP00000314151.1:p.Leu148Gln
ENST00000326003.6:c.443T>A	ENSP00000314151.1:p.Leu148Gln
ENST00000360617.7:c.443T>A	ENSP00000353829.2:p.Leu148Gln
ENST00000422986.6:c.*99T>A	ENSP00000393628.2:n.*99T>A
ENST00000593997.5:c.443T>A	ENSP00000472907.1:p.Leu148Gln
ENST00000595392.5:c.353-34T>A	ENSP00000468912.1:n.353-34T>A
ENST00000595952.5:c.314T>A	ENSP00000471155.1:p.Leu105Gln
ENST00000596185.5:c.*551T>A	ENSP00000471648.1:n.*551T>A
ENST00000596333.1:n.478T>A
ENST00000597286.5:c.332T>A	ENSP00000470523.1:p.Leu111Gln
ENST00000597483.5:c.314T>A	ENSP00000472411.1:p.Leu105Gln
ENST00000598145.1:c.427T>A
ENST00000601349.5:n.1722T>A
ENST00000601503.5:c.386T>A	ENSP00000472213.1:p.Leu129Gln
ENST00000601812.1:n.875T>A
ENST00000617027.4:c.354-34T>A	ENSP00000483513.1:n.354-34T>A
NM_001030047.1:c.443T>A	NP_001025218.1:p.Leu148Gln
NM_001030048.1:c.314T>A	NP_001025219.1:p.Leu105Gln
NM_001648.2:c.443T>A MANE Select	NP_001639.1:p.Leu148Gln
XM_011526923.1:c.443T>A	XP_011525225.1:p.Leu148Gln
XM_011526924.1:c.443T>A	XP_011525226.1:p.Leu148Gln
XR_935817.1:n.478T>A