Canonical Allele Identifier: CA407022762
Gene: KLK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50858271C>A , CM000681.2:g.50858271C>A GRCh38
NC_000019.9:g.51361527C>A , CM000681.1:g.51361527C>A GRCh37
NC_000019.8:g.56053339C>A NCBI36
NG_011653.1:g.8357C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.449C>A MANE Select ENSP00000314151.1:p.Thr150Asn
ENST00000326003.6:c.449C>A ENSP00000314151.1:p.Thr150Asn
ENST00000360617.7:c.449C>A ENSP00000353829.2:p.Thr150Asn
ENST00000422986.6:c.*105C>A ENSP00000393628.2:n.*105C>A
ENST00000593997.5:c.449C>A ENSP00000472907.1:p.Thr150Asn
ENST00000595392.5:c.353-28C>A ENSP00000468912.1:n.353-28C>A
ENST00000595952.5:c.320C>A ENSP00000471155.1:p.Thr107Asn
ENST00000596185.5:c.*557C>A ENSP00000471648.1:n.*557C>A
ENST00000596333.1:n.484C>A
ENST00000597286.5:c.338C>A ENSP00000470523.1:p.Thr113Asn
ENST00000597483.5:c.320C>A ENSP00000472411.1:p.Thr107Asn
ENST00000598145.1:c.433C>A
ENST00000601349.5:n.1728C>A
ENST00000601503.5:c.392C>A ENSP00000472213.1:p.Thr131Asn
ENST00000601812.1:n.881C>A
ENST00000617027.4:c.354-28C>A ENSP00000483513.1:n.354-28C>A
NM_001030047.1:c.449C>A NP_001025218.1:p.Thr150Asn
NM_001030048.1:c.320C>A NP_001025219.1:p.Thr107Asn
NM_001648.2:c.449C>A MANE Select NP_001639.1:p.Thr150Asn
XM_011526923.1:c.449C>A XP_011525225.1:p.Thr150Asn
XM_011526924.1:c.449C>A XP_011525226.1:p.Thr150Asn
XR_935817.1:n.484C>A