Canonical Allele Identifier: CA407022755

Gene: KLK3

Linked Data

• COSMIC: COSM713241 ; COSM713242
• MyVariant Identifiers: chr19:g.51361523G>T (hg19) ; chr19:g.50858267G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858267G>T , CM000681.2:g.50858267G>T	GRCh38
NC_000019.9:g.51361523G>T , CM000681.1:g.51361523G>T	GRCh37
NC_000019.8:g.56053335G>T	NCBI36
NG_011653.1:g.8353G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.445G>T MANE Select	ENSP00000314151.1:p.Gly149Trp
ENST00000326003.6:c.445G>T	ENSP00000314151.1:p.Gly149Trp
ENST00000360617.7:c.445G>T	ENSP00000353829.2:p.Gly149Trp
ENST00000422986.6:c.*101G>T	ENSP00000393628.2:n.*101G>T
ENST00000593997.5:c.445G>T	ENSP00000472907.1:p.Gly149Trp
ENST00000595392.5:c.353-32G>T	ENSP00000468912.1:n.353-32G>T
ENST00000595952.5:c.316G>T	ENSP00000471155.1:p.Gly106Trp
ENST00000596185.5:c.*553G>T	ENSP00000471648.1:n.*553G>T
ENST00000596333.1:n.480G>T
ENST00000597286.5:c.334G>T	ENSP00000470523.1:p.Gly112Trp
ENST00000597483.5:c.316G>T	ENSP00000472411.1:p.Gly106Trp
ENST00000598145.1:c.429G>T
ENST00000601349.5:n.1724G>T
ENST00000601503.5:c.388G>T	ENSP00000472213.1:p.Gly130Trp
ENST00000601812.1:n.877G>T
ENST00000617027.4:c.354-32G>T	ENSP00000483513.1:n.354-32G>T
NM_001030047.1:c.445G>T	NP_001025218.1:p.Gly149Trp
NM_001030048.1:c.316G>T	NP_001025219.1:p.Gly106Trp
NM_001648.2:c.445G>T MANE Select	NP_001639.1:p.Gly149Trp
XM_011526923.1:c.445G>T	XP_011525225.1:p.Gly149Trp
XM_011526924.1:c.445G>T	XP_011525226.1:p.Gly149Trp
XR_935817.1:n.480G>T