Canonical Allele Identifier: CA633715902

Gene: KLK15

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50826461C>G , CM000681.2:g.50826461C>G	GRCh38
NC_000019.9:g.51329717C>G , CM000681.1:g.51329717C>G	GRCh37
NC_000019.8:g.56021529C>G	NCBI36
NG_012094.1:g.2327G>C
NG_029894.1:g.10063G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000598239.6:c.618+160G>C MANE Select	ENSP00000469315.1:n.618+160G>C
ENST00000695963.1:n.346+160G>C
ENST00000695964.1:n.210-513G>C
ENST00000695965.1:c.364-513G>C	ENSP00000512291.1:n.364-513G>C
ENST00000695998.1:c.615+160G>C	ENSP00000512319.1:n.615+160G>C
ENST00000326856.8:c.615+160G>C	ENSP00000314783.4:n.615+160G>C
ENST00000596531.1:n.691G>C
ENST00000596931.5:c.478+417G>C	ENSP00000471164.1:n.478+417G>C
ENST00000598239.5:c.618+160G>C	ENSP00000469315.1:n.618+160G>C
ENST00000601680.1:n.738+160G>C
ENST00000602114.1:c.*134+160G>C	ENSP00000468856.1:n.*134+160G>C
NM_001277081.1:c.615+160G>C	NP_001264010.1:n.615+160G>C
NM_001277082.1:c.478+417G>C	NP_001264011.1:n.478+417G>C
NM_017509.3:c.618+160G>C	NP_059979.2:n.618+160G>C
NR_102274.1:n.528+160G>C
XM_006723265.2:c.618+160G>C	XP_006723328.1:n.618+160G>C
XM_011527083.1:c.618+160G>C	XP_011525385.1:n.618+160G>C
XM_011527084.1:c.618+160G>C	XP_011525386.1:n.618+160G>C
XM_011527085.1:c.615+160G>C	XP_011525387.1:n.615+160G>C
XM_011527086.1:c.615+160G>C	XP_011525388.1:n.615+160G>C
XM_011527087.1:c.364-513G>C	XP_011525389.1:n.364-513G>C
XM_011527088.1:c.481+417G>C	XP_011525390.1:n.481+417G>C
XM_011527089.1:c.478+417G>C	XP_011525391.1:n.478+417G>C
XM_011527090.1:c.618+160G>C	XP_011525392.1:n.618+160G>C
XM_006723265.3:c.618+160G>C	XP_006723328.1:n.618+160G>C
XM_011527085.2:c.615+160G>C	XP_011525387.1:n.615+160G>C
XM_011527087.2:c.364-513G>C	XP_011525389.1:n.364-513G>C
XM_011527088.2:c.481+417G>C	XP_011525390.1:n.481+417G>C
XM_011527089.2:c.478+417G>C	XP_011525391.1:n.478+417G>C
XR_001753713.1:n.1339+160G>C
NM_001277081.2:c.615+160G>C	NP_001264010.1:n.615+160G>C
NM_001277082.2:c.478+417G>C	NP_001264011.1:n.478+417G>C
NM_017509.4:c.618+160G>C MANE Select	NP_059979.2:n.618+160G>C