Canonical Allele Identifier: CA9604583
Gene: KLK3 HGNC NCBI

Linked Data

dbSNP Id: rs764929426

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50859974T>A , CM000681.2:g.50859974T>A GRCh38
NC_000019.9:g.51363230T>A , CM000681.1:g.51363230T>A GRCh37
NC_000019.8:g.56055042T>A NCBI36
NG_011653.1:g.10060T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.633T>A MANE Select ENSP00000314151.1:p.Gly211=
ENST00000326003.6:c.633T>A ENSP00000314151.1:p.Gly211=
ENST00000360617.7:c.1075T>A ENSP00000353829.2:n.1075T>A
ENST00000422986.6:c.*289T>A ENSP00000393628.2:n.*289T>A
ENST00000595392.5:c.*134T>A ENSP00000468912.1:n.*134T>A
ENST00000595952.5:c.504T>A ENSP00000471155.1:p.Gly168=
ENST00000596185.5:c.*741T>A ENSP00000471648.1:n.*741T>A
ENST00000596333.1:n.811T>A
ENST00000598145.1:c.635T>A
ENST00000601349.5:n.1912T>A
ENST00000601812.1:n.1065T>A
ENST00000617027.4:c.510T>A ENSP00000483513.1:p.Gly170=
NM_001030047.1:c.*358T>A NP_001025218.1:n.*358T>A
NM_001030048.1:c.504T>A NP_001025219.1:p.Gly168=
NM_001648.2:c.633T>A MANE Select NP_001639.1:p.Gly211=
XM_011526923.1:c.651T>A XP_011525225.1:p.Gly217=
XM_011526924.1:c.*358T>A XP_011525226.1:n.*358T>A
XR_935817.1:n.1324+720T>A