Canonical Allele Identifier: CA14646643
Gene: KLK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50909070C>G , CM000681.2:g.50909070C>G GRCh38
NC_000019.9:g.51412326C>G , CM000681.1:g.51412326C>G GRCh37
NC_000019.8:g.56104138C>G NCBI36
NG_012154.2:g.6669G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000324041.6:c.224+182G>C MANE Select ENSP00000326159.1:n.224+182G>C
ENST00000324041.5:c.224+182G>C ENSP00000326159.1:n.224+182G>C
ENST00000431178.2:c.77+182G>C ENSP00000399448.2:n.77+182G>C
ENST00000593885.1:c.-119G>C ENSP00000469769.1:n.-119G>C
ENST00000596876.1:n.143+170G>C
ENST00000598305.5:c.-62+170G>C ENSP00000469963.1:n.-62+170G>C
ENST00000599865.5:n.77+182G>C
ENST00000602148.1:c.236+170G>C ENSP00000472091.1:n.236+170G>C
NM_001302961.1:c.-62+170G>C NP_001289890.1:n.-62+170G>C
NM_004917.4:c.224+182G>C NP_004908.4:n.224+182G>C
NR_126566.1:n.217+170G>C
XM_005259441.3:c.-119G>C XP_005259498.2:n.-119G>C
XM_011527545.1:c.224+182G>C XP_011525847.1:n.224+182G>C
XM_011527546.1:c.224+182G>C XP_011525848.1:n.224+182G>C
XM_011527547.1:c.77+182G>C XP_011525849.1:n.77+182G>C
XM_005259441.4:c.-119G>C XP_005259498.2:n.-119G>C
XM_011527545.3:c.224+182G>C XP_011525847.1:n.224+182G>C
XM_011527546.2:c.224+182G>C XP_011525848.1:n.224+182G>C
NM_001302961.2:c.-62+170G>C NP_001289890.1:n.-62+170G>C
NR_126566.2:n.217+170G>C
NM_004917.5:c.224+182G>C MANE Select NP_004908.4:n.224+182G>C