Canonical Allele Identifier: CA407041543
Gene: KLK4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908671T>A , CM000681.2:g.50908671T>A GRCh38
NC_000019.9:g.51411927T>A , CM000681.1:g.51411927T>A GRCh37
NC_000019.8:g.56103739T>A NCBI36
NG_012154.2:g.7068A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000324041.6:c.383A>T MANE Select ENSP00000326159.1:p.Glu128Val
ENST00000324041.5:c.383A>T ENSP00000326159.1:p.Glu128Val
ENST00000431178.2:c.236A>T ENSP00000399448.2:p.Glu79Val
ENST00000593885.1:c.98A>T ENSP00000469769.1:p.Glu33Val
ENST00000596876.1:n.302A>T
ENST00000598305.5:c.98A>T ENSP00000469963.1:p.Glu33Val
ENST00000599865.5:n.236A>T
ENST00000602148.1:c.395A>T ENSP00000472091.1:n.395A>T
NM_001302961.1:c.98A>T NP_001289890.1:p.Glu33Val
NM_004917.4:c.383A>T NP_004908.4:p.Glu128Val
NR_126566.1:n.376A>T
XM_005259441.3:c.98A>T XP_005259498.2:p.Glu33Val
XM_011527545.1:c.383A>T XP_011525847.1:p.Glu128Val
XM_011527546.1:c.383A>T XP_011525848.1:p.Glu128Val
XM_011527547.1:c.236A>T XP_011525849.1:p.Glu79Val
XM_005259441.4:c.98A>T XP_005259498.2:p.Glu33Val
XM_011527545.3:c.383A>T XP_011525847.1:p.Glu128Val
XM_011527546.2:c.383A>T XP_011525848.1:p.Glu128Val
NM_001302961.2:c.98A>T NP_001289890.1:p.Glu33Val
NR_126566.2:n.376A>T
NM_004917.5:c.383A>T MANE Select NP_004908.4:p.Glu128Val