Canonical Allele Identifier: CA2582241029
Gene: KLK15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50832628T>A , CM000681.2:g.50832628T>A GRCh38
NC_000019.9:g.51335884T>A , CM000681.1:g.51335884T>A GRCh37
NC_000019.8:g.56027696T>A NCBI36
NG_029894.1:g.3896A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000598239.6:c.-32+899A>T MANE Select ENSP00000469315.1:n.-32+899A>T
ENST00000695965.1:c.-32+899A>T ENSP00000512291.1:n.-32+899A>T
ENST00000695998.1:c.-32+471A>T ENSP00000512319.1:n.-32+471A>T
ENST00000326856.8:c.-31-1105A>T ENSP00000314783.4:n.-31-1105A>T
ENST00000598673.1:c.-156+471A>T ENSP00000472523.1:n.-156+471A>T
NR_131203.1:n.213+1335T>A
NR_131205.1:n.230+1335T>A
XM_006723265.2:c.-32+899A>T XP_006723328.1:n.-32+899A>T
XM_011527083.1:c.-31-1105A>T XP_011525385.1:n.-31-1105A>T
XM_011527084.1:c.-32+471A>T XP_011525386.1:n.-32+471A>T
XM_011527085.1:c.-32+899A>T XP_011525387.1:n.-32+899A>T
XM_011527086.1:c.-32+471A>T XP_011525388.1:n.-32+471A>T
XM_011527087.1:c.-32+899A>T XP_011525389.1:n.-32+899A>T
XM_011527088.1:c.-32+899A>T XP_011525390.1:n.-32+899A>T
XM_011527089.1:c.-32+899A>T XP_011525391.1:n.-32+899A>T
XM_011527090.1:c.-31-1105A>T XP_011525392.1:n.-31-1105A>T
XR_936030.1:n.298+1335T>A
XR_936031.1:n.298+1335T>A
XR_936032.1:n.298+1335T>A
XR_936033.1:n.294+1335T>A
XR_936035.1:n.281+1335T>A
XM_006723265.3:c.-32+899A>T XP_006723328.1:n.-32+899A>T
XM_011527085.2:c.-32+899A>T XP_011525387.1:n.-32+899A>T
XM_011527087.2:c.-32+899A>T XP_011525389.1:n.-32+899A>T
XM_011527088.2:c.-32+899A>T XP_011525390.1:n.-32+899A>T
XM_011527089.2:c.-32+899A>T XP_011525391.1:n.-32+899A>T
XM_017026943.1:c.-32+899A>T XP_016882432.1:n.-32+899A>T
XR_001753713.1:n.811+899A>T
NM_001277081.2:c.-32+899A>T NP_001264010.1:n.-32+899A>T
NM_001277082.2:c.-32+899A>T NP_001264011.1:n.-32+899A>T
NM_017509.4:c.-32+899A>T MANE Select NP_059979.2:n.-32+899A>T