Canonical Allele Identifier: CA508313515
Gene: KLK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.51361336A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50858080A>T , CM000681.2:g.50858080A>T GRCh38
NC_000019.9:g.51361336A>T , CM000681.1:g.51361336A>T GRCh37
NC_000019.8:g.56053148A>T NCBI36
NG_011653.1:g.8166A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.258A>T MANE Select ENSP00000314151.1:p.Thr86=
ENST00000326003.6:c.258A>T ENSP00000314151.1:p.Thr86=
ENST00000360617.7:c.258A>T ENSP00000353829.2:p.Thr86=
ENST00000422986.6:c.258A>T ENSP00000393628.2:p.Thr86=
ENST00000593997.5:c.258A>T ENSP00000472907.1:p.Thr86=
ENST00000595392.5:c.258A>T ENSP00000468912.1:p.Thr86=
ENST00000595952.5:c.207-78A>T ENSP00000471155.1:n.207-78A>T
ENST00000596185.5:c.*366A>T ENSP00000471648.1:n.*366A>T
ENST00000596333.1:n.293A>T
ENST00000597286.5:c.147A>T ENSP00000470523.1:p.Thr49=
ENST00000597483.5:c.207-78A>T ENSP00000472411.1:n.207-78A>T
ENST00000598145.1:c.242A>T
ENST00000601349.5:n.1537A>T
ENST00000601503.5:c.201A>T ENSP00000472213.1:p.Thr67=
ENST00000601812.1:n.690A>T
ENST00000617027.4:c.258A>T ENSP00000483513.1:p.Thr86=
NM_001030047.1:c.258A>T NP_001025218.1:p.Thr86=
NM_001030048.1:c.207-78A>T NP_001025219.1:n.207-78A>T
NM_001648.2:c.258A>T MANE Select NP_001639.1:p.Thr86=
XM_011526923.1:c.258A>T XP_011525225.1:p.Thr86=
XM_011526924.1:c.258A>T XP_011525226.1:p.Thr86=
XR_935817.1:n.293A>T