Canonical Allele Identifier: CA407022267
Gene: KLK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50858124A>T , CM000681.2:g.50858124A>T GRCh38
NC_000019.9:g.51361380A>T , CM000681.1:g.51361380A>T GRCh37
NC_000019.8:g.56053192A>T NCBI36
NG_011653.1:g.8210A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.302A>T MANE Select ENSP00000314151.1:p.Tyr101Phe
ENST00000326003.6:c.302A>T ENSP00000314151.1:p.Tyr101Phe
ENST00000360617.7:c.302A>T ENSP00000353829.2:p.Tyr101Phe
ENST00000422986.6:c.265-34A>T ENSP00000393628.2:n.265-34A>T
ENST00000593997.5:c.302A>T ENSP00000472907.1:p.Tyr101Phe
ENST00000595392.5:c.302A>T ENSP00000468912.1:p.Tyr101Phe
ENST00000595952.5:c.207-34A>T ENSP00000471155.1:n.207-34A>T
ENST00000596185.5:c.*410A>T ENSP00000471648.1:n.*410A>T
ENST00000596333.1:n.337A>T
ENST00000597286.5:c.191A>T ENSP00000470523.1:p.Tyr64Phe
ENST00000597483.5:c.207-34A>T ENSP00000472411.1:n.207-34A>T
ENST00000598145.1:c.286A>T
ENST00000601349.5:n.1581A>T
ENST00000601503.5:c.245A>T ENSP00000472213.1:p.Tyr82Phe
ENST00000601812.1:n.734A>T
ENST00000617027.4:c.302A>T ENSP00000483513.1:p.Tyr101Phe
NM_001030047.1:c.302A>T NP_001025218.1:p.Tyr101Phe
NM_001030048.1:c.207-34A>T NP_001025219.1:n.207-34A>T
NM_001648.2:c.302A>T MANE Select NP_001639.1:p.Tyr101Phe
XM_011526923.1:c.302A>T XP_011525225.1:p.Tyr101Phe
XM_011526924.1:c.302A>T XP_011525226.1:p.Tyr101Phe
XR_935817.1:n.337A>T