Canonical Allele Identifier: CA508313707

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51361522G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858266G>T , CM000681.2:g.50858266G>T	GRCh38
NC_000019.9:g.51361522G>T , CM000681.1:g.51361522G>T	GRCh37
NC_000019.8:g.56053334G>T	NCBI36
NG_011653.1:g.8352G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.444G>T MANE Select	ENSP00000314151.1:p.Leu148=
ENST00000326003.6:c.444G>T	ENSP00000314151.1:p.Leu148=
ENST00000360617.7:c.444G>T	ENSP00000353829.2:p.Leu148=
ENST00000422986.6:c.*100G>T	ENSP00000393628.2:n.*100G>T
ENST00000593997.5:c.444G>T	ENSP00000472907.1:p.Leu148=
ENST00000595392.5:c.353-33G>T	ENSP00000468912.1:n.353-33G>T
ENST00000595952.5:c.315G>T	ENSP00000471155.1:p.Leu105=
ENST00000596185.5:c.*552G>T	ENSP00000471648.1:n.*552G>T
ENST00000596333.1:n.479G>T
ENST00000597286.5:c.333G>T	ENSP00000470523.1:p.Leu111=
ENST00000597483.5:c.315G>T	ENSP00000472411.1:p.Leu105=
ENST00000598145.1:c.428G>T
ENST00000601349.5:n.1723G>T
ENST00000601503.5:c.387G>T	ENSP00000472213.1:p.Leu129=
ENST00000601812.1:n.876G>T
ENST00000617027.4:c.354-33G>T	ENSP00000483513.1:n.354-33G>T
NM_001030047.1:c.444G>T	NP_001025218.1:p.Leu148=
NM_001030048.1:c.315G>T	NP_001025219.1:p.Leu105=
NM_001648.2:c.444G>T MANE Select	NP_001639.1:p.Leu148=
XM_011526923.1:c.444G>T	XP_011525225.1:p.Leu148=
XM_011526924.1:c.444G>T	XP_011525226.1:p.Leu148=
XR_935817.1:n.479G>T