Canonical Allele Identifier: CA2567191478

Gene: KLK15

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50832682T>G , CM000681.2:g.50832682T>G	GRCh38
NC_000019.9:g.51335938T>G , CM000681.1:g.51335938T>G	GRCh37
NC_000019.8:g.56027750T>G	NCBI36
NG_029894.1:g.3842A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000598239.6:c.-32+845A>C MANE Select	ENSP00000469315.1:n.-32+845A>C
ENST00000695965.1:c.-32+845A>C	ENSP00000512291.1:n.-32+845A>C
ENST00000695998.1:c.-32+417A>C	ENSP00000512319.1:n.-32+417A>C
ENST00000326856.8:c.-31-1159A>C	ENSP00000314783.4:n.-31-1159A>C
ENST00000598673.1:c.-156+417A>C	ENSP00000472523.1:n.-156+417A>C
NR_131203.1:n.213+1389T>G
NR_131205.1:n.230+1389T>G
XM_006723265.2:c.-32+845A>C	XP_006723328.1:n.-32+845A>C
XM_011527083.1:c.-31-1159A>C	XP_011525385.1:n.-31-1159A>C
XM_011527084.1:c.-32+417A>C	XP_011525386.1:n.-32+417A>C
XM_011527085.1:c.-32+845A>C	XP_011525387.1:n.-32+845A>C
XM_011527086.1:c.-32+417A>C	XP_011525388.1:n.-32+417A>C
XM_011527087.1:c.-32+845A>C	XP_011525389.1:n.-32+845A>C
XM_011527088.1:c.-32+845A>C	XP_011525390.1:n.-32+845A>C
XM_011527089.1:c.-32+845A>C	XP_011525391.1:n.-32+845A>C
XM_011527090.1:c.-31-1159A>C	XP_011525392.1:n.-31-1159A>C
XR_936030.1:n.298+1389T>G
XR_936031.1:n.298+1389T>G
XR_936032.1:n.298+1389T>G
XR_936033.1:n.294+1389T>G
XR_936035.1:n.281+1389T>G
XM_006723265.3:c.-32+845A>C	XP_006723328.1:n.-32+845A>C
XM_011527085.2:c.-32+845A>C	XP_011525387.1:n.-32+845A>C
XM_011527087.2:c.-32+845A>C	XP_011525389.1:n.-32+845A>C
XM_011527088.2:c.-32+845A>C	XP_011525390.1:n.-32+845A>C
XM_011527089.2:c.-32+845A>C	XP_011525391.1:n.-32+845A>C
XM_017026943.1:c.-32+845A>C	XP_016882432.1:n.-32+845A>C
XR_001753713.1:n.811+845A>C
NM_001277081.2:c.-32+845A>C	NP_001264010.1:n.-32+845A>C
NM_001277082.2:c.-32+845A>C	NP_001264011.1:n.-32+845A>C
NM_017509.4:c.-32+845A>C MANE Select	NP_059979.2:n.-32+845A>C