Canonical Allele Identifier: CA407022702
Gene: KLK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50858246C>T , CM000681.2:g.50858246C>T GRCh38
NC_000019.9:g.51361502C>T , CM000681.1:g.51361502C>T GRCh37
NC_000019.8:g.56053314C>T NCBI36
NG_011653.1:g.8332C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.424C>T MANE Select ENSP00000314151.1:p.Pro142Ser
ENST00000326003.6:c.424C>T ENSP00000314151.1:p.Pro142Ser
ENST00000360617.7:c.424C>T ENSP00000353829.2:p.Pro142Ser
ENST00000422986.6:c.*80C>T ENSP00000393628.2:n.*80C>T
ENST00000593997.5:c.424C>T ENSP00000472907.1:p.Pro142Ser
ENST00000595392.5:c.353-53C>T ENSP00000468912.1:n.353-53C>T
ENST00000595952.5:c.295C>T ENSP00000471155.1:p.Pro99Ser
ENST00000596185.5:c.*532C>T ENSP00000471648.1:n.*532C>T
ENST00000596333.1:n.459C>T
ENST00000597286.5:c.313C>T ENSP00000470523.1:p.Pro105Ser
ENST00000597483.5:c.295C>T ENSP00000472411.1:p.Pro99Ser
ENST00000598145.1:c.408C>T
ENST00000601349.5:n.1703C>T
ENST00000601503.5:c.367C>T ENSP00000472213.1:p.Pro123Ser
ENST00000601812.1:n.856C>T
ENST00000617027.4:c.354-53C>T ENSP00000483513.1:n.354-53C>T
NM_001030047.1:c.424C>T NP_001025218.1:p.Pro142Ser
NM_001030048.1:c.295C>T NP_001025219.1:p.Pro99Ser
NM_001648.2:c.424C>T MANE Select NP_001639.1:p.Pro142Ser
XM_011526923.1:c.424C>T XP_011525225.1:p.Pro142Ser
XM_011526924.1:c.424C>T XP_011525226.1:p.Pro142Ser
XR_935817.1:n.459C>T