Canonical Allele Identifier: CA407022246

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51361373C>A (hg19) ; chr19:g.50858117C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858117C>A , CM000681.2:g.50858117C>A	GRCh38
NC_000019.9:g.51361373C>A , CM000681.1:g.51361373C>A	GRCh37
NC_000019.8:g.56053185C>A	NCBI36
NG_011653.1:g.8203C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.295C>A MANE Select	ENSP00000314151.1:p.Pro99Thr
ENST00000326003.6:c.295C>A	ENSP00000314151.1:p.Pro99Thr
ENST00000360617.7:c.295C>A	ENSP00000353829.2:p.Pro99Thr
ENST00000422986.6:c.264+31C>A	ENSP00000393628.2:n.264+31C>A
ENST00000593997.5:c.295C>A	ENSP00000472907.1:p.Pro99Thr
ENST00000595392.5:c.295C>A	ENSP00000468912.1:p.Pro99Thr
ENST00000595952.5:c.207-41C>A	ENSP00000471155.1:n.207-41C>A
ENST00000596185.5:c.*403C>A	ENSP00000471648.1:n.*403C>A
ENST00000596333.1:n.330C>A
ENST00000597286.5:c.184C>A	ENSP00000470523.1:p.Pro62Thr
ENST00000597483.5:c.207-41C>A	ENSP00000472411.1:n.207-41C>A
ENST00000598145.1:c.279C>A
ENST00000601349.5:n.1574C>A
ENST00000601503.5:c.238C>A	ENSP00000472213.1:p.Pro80Thr
ENST00000601812.1:n.727C>A
ENST00000617027.4:c.295C>A	ENSP00000483513.1:p.Pro99Thr
NM_001030047.1:c.295C>A	NP_001025218.1:p.Pro99Thr
NM_001030048.1:c.207-41C>A	NP_001025219.1:n.207-41C>A
NM_001648.2:c.295C>A MANE Select	NP_001639.1:p.Pro99Thr
XM_011526923.1:c.295C>A	XP_011525225.1:p.Pro99Thr
XM_011526924.1:c.295C>A	XP_011525226.1:p.Pro99Thr
XR_935817.1:n.330C>A