Canonical Allele Identifier: CA407040784
Gene: KLK4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908448C>T , CM000681.2:g.50908448C>T GRCh38
NC_000019.9:g.51411704C>T , CM000681.1:g.51411704C>T GRCh37
NC_000019.8:g.56103516C>T NCBI36
NG_012154.2:g.7291G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000324041.6:c.523G>A MANE Select ENSP00000326159.1:p.Glu175Lys
ENST00000324041.5:c.523G>A ENSP00000326159.1:p.Glu175Lys
ENST00000431178.2:c.328+131G>A ENSP00000399448.2:n.328+131G>A
ENST00000593885.1:c.*18G>A ENSP00000469769.1:n.*18G>A
ENST00000596876.1:n.525G>A
ENST00000598305.5:c.*18G>A ENSP00000469963.1:n.*18G>A
ENST00000599865.5:n.459G>A
ENST00000602148.1:c.535G>A ENSP00000472091.1:n.535G>A
NM_001302961.1:c.238G>A NP_001289890.1:p.Glu80Lys
NM_004917.4:c.523G>A NP_004908.4:p.Glu175Lys
NR_126566.1:n.512G>A
XM_005259441.3:c.238G>A XP_005259498.2:p.Glu80Lys
XM_011527545.1:c.*18G>A XP_011525847.1:n.*18G>A
XM_011527546.1:c.475+131G>A XP_011525848.1:n.475+131G>A
XM_011527547.1:c.376G>A XP_011525849.1:p.Glu126Lys
XM_005259441.4:c.238G>A XP_005259498.2:p.Glu80Lys
XM_011527545.3:c.*18G>A XP_011525847.1:n.*18G>A
XM_011527546.2:c.475+131G>A XP_011525848.1:n.475+131G>A
NM_001302961.2:c.238G>A NP_001289890.1:p.Glu80Lys
NR_126566.2:n.512G>A
NM_004917.5:c.523G>A MANE Select NP_004908.4:p.Glu175Lys