Canonical Allele Identifier: CA508313613

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51361417A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858161A>T , CM000681.2:g.50858161A>T	GRCh38
NC_000019.9:g.51361417A>T , CM000681.1:g.51361417A>T	GRCh37
NC_000019.8:g.56053229A>T	NCBI36
NG_011653.1:g.8247A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.339A>T MANE Select	ENSP00000314151.1:p.Pro113=
ENST00000326003.6:c.339A>T	ENSP00000314151.1:p.Pro113=
ENST00000360617.7:c.339A>T	ENSP00000353829.2:p.Pro113=
ENST00000422986.6:c.268A>T	ENSP00000393628.2:p.Arg90Trp
ENST00000593997.5:c.339A>T	ENSP00000472907.1:p.Pro113=
ENST00000595392.5:c.339A>T	ENSP00000468912.1:p.Pro113=
ENST00000595952.5:c.210A>T	ENSP00000471155.1:p.Pro70=
ENST00000596185.5:c.*447A>T	ENSP00000471648.1:n.*447A>T
ENST00000596333.1:n.374A>T
ENST00000597286.5:c.228A>T	ENSP00000470523.1:p.Pro76=
ENST00000597483.5:c.210A>T	ENSP00000472411.1:p.Pro70=
ENST00000598145.1:c.323A>T
ENST00000601349.5:n.1618A>T
ENST00000601503.5:c.282A>T	ENSP00000472213.1:p.Pro94=
ENST00000601812.1:n.771A>T
ENST00000617027.4:c.339A>T	ENSP00000483513.1:p.Pro113=
NM_001030047.1:c.339A>T	NP_001025218.1:p.Pro113=
NM_001030048.1:c.210A>T	NP_001025219.1:p.Pro70=
NM_001648.2:c.339A>T MANE Select	NP_001639.1:p.Pro113=
XM_011526923.1:c.339A>T	XP_011525225.1:p.Pro113=
XM_011526924.1:c.339A>T	XP_011525226.1:p.Pro113=
XR_935817.1:n.374A>T