Canonical Allele Identifier: CA407022634
Gene: KLK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50858229T>A , CM000681.2:g.50858229T>A GRCh38
NC_000019.9:g.51361485T>A , CM000681.1:g.51361485T>A GRCh37
NC_000019.8:g.56053297T>A NCBI36
NG_011653.1:g.8315T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.407T>A MANE Select ENSP00000314151.1:p.Val136Glu
ENST00000326003.6:c.407T>A ENSP00000314151.1:p.Val136Glu
ENST00000360617.7:c.407T>A ENSP00000353829.2:p.Val136Glu
ENST00000422986.6:c.*63T>A ENSP00000393628.2:n.*63T>A
ENST00000593997.5:c.407T>A ENSP00000472907.1:p.Val136Glu
ENST00000595392.5:c.352+55T>A ENSP00000468912.1:n.352+55T>A
ENST00000595952.5:c.278T>A ENSP00000471155.1:p.Val93Glu
ENST00000596185.5:c.*515T>A ENSP00000471648.1:n.*515T>A
ENST00000596333.1:n.442T>A
ENST00000597286.5:c.296T>A ENSP00000470523.1:p.Val99Glu
ENST00000597483.5:c.278T>A ENSP00000472411.1:p.Val93Glu
ENST00000598145.1:c.391T>A
ENST00000601349.5:n.1686T>A
ENST00000601503.5:c.350T>A ENSP00000472213.1:p.Val117Glu
ENST00000601812.1:n.839T>A
ENST00000617027.4:c.353+54T>A ENSP00000483513.1:n.353+54T>A
NM_001030047.1:c.407T>A NP_001025218.1:p.Val136Glu
NM_001030048.1:c.278T>A NP_001025219.1:p.Val93Glu
NM_001648.2:c.407T>A MANE Select NP_001639.1:p.Val136Glu
XM_011526923.1:c.407T>A XP_011525225.1:p.Val136Glu
XM_011526924.1:c.407T>A XP_011525226.1:p.Val136Glu
XR_935817.1:n.442T>A