Canonical Allele Identifier: CA508313662
Gene: KLK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.51361459A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50858203A>T , CM000681.2:g.50858203A>T GRCh38
NC_000019.9:g.51361459A>T , CM000681.1:g.51361459A>T GRCh37
NC_000019.8:g.56053271A>T NCBI36
NG_011653.1:g.8289A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.381A>T MANE Select ENSP00000314151.1:p.Ser127=
ENST00000326003.6:c.381A>T ENSP00000314151.1:p.Ser127=
ENST00000360617.7:c.381A>T ENSP00000353829.2:p.Ser127=
ENST00000422986.6:c.*37A>T ENSP00000393628.2:n.*37A>T
ENST00000593997.5:c.381A>T ENSP00000472907.1:p.Ser127=
ENST00000595392.5:c.352+29A>T ENSP00000468912.1:n.352+29A>T
ENST00000595952.5:c.252A>T ENSP00000471155.1:p.Ser84=
ENST00000596185.5:c.*489A>T ENSP00000471648.1:n.*489A>T
ENST00000596333.1:n.416A>T
ENST00000597286.5:c.270A>T ENSP00000470523.1:p.Ser90=
ENST00000597483.5:c.252A>T ENSP00000472411.1:p.Ser84=
ENST00000598145.1:c.365A>T
ENST00000601349.5:n.1660A>T
ENST00000601503.5:c.324A>T ENSP00000472213.1:p.Ser108=
ENST00000601812.1:n.813A>T
ENST00000617027.4:c.353+28A>T ENSP00000483513.1:n.353+28A>T
NM_001030047.1:c.381A>T NP_001025218.1:p.Ser127=
NM_001030048.1:c.252A>T NP_001025219.1:p.Ser84=
NM_001648.2:c.381A>T MANE Select NP_001639.1:p.Ser127=
XM_011526923.1:c.381A>T XP_011525225.1:p.Ser127=
XM_011526924.1:c.381A>T XP_011525226.1:p.Ser127=
XR_935817.1:n.416A>T