Canonical Allele Identifier: CA2341098349
Gene: KLK15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50825480C>G , CM000681.2:g.50825480C>G GRCh38
NC_000019.9:g.51328736C>G , CM000681.1:g.51328736C>G GRCh37
NC_000019.8:g.56020548C>G NCBI36
NG_012094.1:g.3308G>C
NG_029894.1:g.11044G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000598239.6:c.*316G>C MANE Select ENSP00000469315.1:n.*316G>C
ENST00000695963.1:n.815G>C
ENST00000695964.1:n.678G>C
ENST00000695965.1:c.*316G>C ENSP00000512291.1:n.*316G>C
ENST00000695998.1:c.*316G>C ENSP00000512319.1:n.*316G>C
ENST00000326856.8:c.*316G>C ENSP00000314783.4:n.*316G>C
ENST00000601680.1:n.1207G>C
NM_001277081.1:c.*316G>C NP_001264010.1:n.*316G>C
NM_001277082.1:c.*464G>C NP_001264011.1:n.*464G>C
NM_017509.3:c.*316G>C NP_059979.2:n.*316G>C
NR_102274.1:n.997G>C
XM_006723265.2:c.*316G>C XP_006723328.1:n.*316G>C
XM_011527083.1:c.*316G>C XP_011525385.1:n.*316G>C
XM_011527084.1:c.*316G>C XP_011525386.1:n.*316G>C
XM_011527085.1:c.*316G>C XP_011525387.1:n.*316G>C
XM_011527086.1:c.*316G>C XP_011525388.1:n.*316G>C
XM_011527087.1:c.*316G>C XP_011525389.1:n.*316G>C
XM_011527089.1:c.*464G>C XP_011525391.1:n.*464G>C
XM_011527090.1:c.*316G>C XP_011525392.1:n.*316G>C
XM_006723265.3:c.*316G>C XP_006723328.1:n.*316G>C
XM_011527085.2:c.*316G>C XP_011525387.1:n.*316G>C
XM_011527087.2:c.*316G>C XP_011525389.1:n.*316G>C
XM_011527089.2:c.*464G>C XP_011525391.1:n.*464G>C
XR_001753713.1:n.1808G>C
NM_001277081.2:c.*316G>C NP_001264010.1:n.*316G>C
NM_001277082.2:c.*464G>C NP_001264011.1:n.*464G>C
NM_017509.4:c.*316G>C MANE Select NP_059979.2:n.*316G>C