Canonical Allele Identifier: CA407022252

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51361374C>G (hg19) ; chr19:g.50858118C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858118C>G , CM000681.2:g.50858118C>G	GRCh38
NC_000019.9:g.51361374C>G , CM000681.1:g.51361374C>G	GRCh37
NC_000019.8:g.56053186C>G	NCBI36
NG_011653.1:g.8204C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.296C>G MANE Select	ENSP00000314151.1:p.Pro99Arg
ENST00000326003.6:c.296C>G	ENSP00000314151.1:p.Pro99Arg
ENST00000360617.7:c.296C>G	ENSP00000353829.2:p.Pro99Arg
ENST00000422986.6:c.264+32C>G	ENSP00000393628.2:n.264+32C>G
ENST00000593997.5:c.296C>G	ENSP00000472907.1:p.Pro99Arg
ENST00000595392.5:c.296C>G	ENSP00000468912.1:p.Pro99Arg
ENST00000595952.5:c.207-40C>G	ENSP00000471155.1:n.207-40C>G
ENST00000596185.5:c.*404C>G	ENSP00000471648.1:n.*404C>G
ENST00000596333.1:n.331C>G
ENST00000597286.5:c.185C>G	ENSP00000470523.1:p.Pro62Arg
ENST00000597483.5:c.207-40C>G	ENSP00000472411.1:n.207-40C>G
ENST00000598145.1:c.280C>G
ENST00000601349.5:n.1575C>G
ENST00000601503.5:c.239C>G	ENSP00000472213.1:p.Pro80Arg
ENST00000601812.1:n.728C>G
ENST00000617027.4:c.296C>G	ENSP00000483513.1:p.Pro99Arg
NM_001030047.1:c.296C>G	NP_001025218.1:p.Pro99Arg
NM_001030048.1:c.207-40C>G	NP_001025219.1:n.207-40C>G
NM_001648.2:c.296C>G MANE Select	NP_001639.1:p.Pro99Arg
XM_011526923.1:c.296C>G	XP_011525225.1:p.Pro99Arg
XM_011526924.1:c.296C>G	XP_011525226.1:p.Pro99Arg
XR_935817.1:n.331C>G