Canonical Allele Identifier: CA407022632

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51361484G>C (hg19) ; chr19:g.50858228G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858228G>C , CM000681.2:g.50858228G>C	GRCh38
NC_000019.9:g.51361484G>C , CM000681.1:g.51361484G>C	GRCh37
NC_000019.8:g.56053296G>C	NCBI36
NG_011653.1:g.8314G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.406G>C MANE Select	ENSP00000314151.1:p.Val136Leu
ENST00000326003.6:c.406G>C	ENSP00000314151.1:p.Val136Leu
ENST00000360617.7:c.406G>C	ENSP00000353829.2:p.Val136Leu
ENST00000422986.6:c.*62G>C	ENSP00000393628.2:n.*62G>C
ENST00000593997.5:c.406G>C	ENSP00000472907.1:p.Val136Leu
ENST00000595392.5:c.352+54G>C	ENSP00000468912.1:n.352+54G>C
ENST00000595952.5:c.277G>C	ENSP00000471155.1:p.Val93Leu
ENST00000596185.5:c.*514G>C	ENSP00000471648.1:n.*514G>C
ENST00000596333.1:n.441G>C
ENST00000597286.5:c.295G>C	ENSP00000470523.1:p.Val99Leu
ENST00000597483.5:c.277G>C	ENSP00000472411.1:p.Val93Leu
ENST00000598145.1:c.390G>C
ENST00000601349.5:n.1685G>C
ENST00000601503.5:c.349G>C	ENSP00000472213.1:p.Val117Leu
ENST00000601812.1:n.838G>C
ENST00000617027.4:c.353+53G>C	ENSP00000483513.1:n.353+53G>C
NM_001030047.1:c.406G>C	NP_001025218.1:p.Val136Leu
NM_001030048.1:c.277G>C	NP_001025219.1:p.Val93Leu
NM_001648.2:c.406G>C MANE Select	NP_001639.1:p.Val136Leu
XM_011526923.1:c.406G>C	XP_011525225.1:p.Val136Leu
XM_011526924.1:c.406G>C	XP_011525226.1:p.Val136Leu
XR_935817.1:n.441G>C