Canonical Allele Identifier: CA508313690

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51361501G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858245G>C , CM000681.2:g.50858245G>C	GRCh38
NC_000019.9:g.51361501G>C , CM000681.1:g.51361501G>C	GRCh37
NC_000019.8:g.56053313G>C	NCBI36
NG_011653.1:g.8331G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.423G>C MANE Select	ENSP00000314151.1:p.Leu141=
ENST00000326003.6:c.423G>C	ENSP00000314151.1:p.Leu141=
ENST00000360617.7:c.423G>C	ENSP00000353829.2:p.Leu141=
ENST00000422986.6:c.*79G>C	ENSP00000393628.2:n.*79G>C
ENST00000593997.5:c.423G>C	ENSP00000472907.1:p.Leu141=
ENST00000595392.5:c.353-54G>C	ENSP00000468912.1:n.353-54G>C
ENST00000595952.5:c.294G>C	ENSP00000471155.1:p.Leu98=
ENST00000596185.5:c.*531G>C	ENSP00000471648.1:n.*531G>C
ENST00000596333.1:n.458G>C
ENST00000597286.5:c.312G>C	ENSP00000470523.1:p.Leu104=
ENST00000597483.5:c.294G>C	ENSP00000472411.1:p.Leu98=
ENST00000598145.1:c.407G>C
ENST00000601349.5:n.1702G>C
ENST00000601503.5:c.366G>C	ENSP00000472213.1:p.Leu122=
ENST00000601812.1:n.855G>C
ENST00000617027.4:c.354-54G>C	ENSP00000483513.1:n.354-54G>C
NM_001030047.1:c.423G>C	NP_001025218.1:p.Leu141=
NM_001030048.1:c.294G>C	NP_001025219.1:p.Leu98=
NM_001648.2:c.423G>C MANE Select	NP_001639.1:p.Leu141=
XM_011526923.1:c.423G>C	XP_011525225.1:p.Leu141=
XM_011526924.1:c.423G>C	XP_011525226.1:p.Leu141=
XR_935817.1:n.458G>C