Canonical Allele Identifier: CA2341138404
Gene: KLK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908684C= , CM000681.2:g.50908684C= GRCh38
NC_000019.9:g.51411940C= , CM000681.1:g.51411940C= GRCh37
NC_000019.8:g.56103752C= NCBI36
NG_012154.2:g.7055G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000324041.6:c.370G= MANE Select ENSP00000326159.1:p.Glu124=
ENST00000324041.5:c.370G= ENSP00000326159.1:p.Glu124=
ENST00000431178.2:c.223G= ENSP00000399448.2:p.Glu75=
ENST00000593885.1:c.85G= ENSP00000469769.1:p.Glu29=
ENST00000596876.1:n.289G=
ENST00000598305.5:c.85G= ENSP00000469963.1:p.Glu29=
ENST00000599865.5:n.223G=
ENST00000602148.1:c.382G= ENSP00000472091.1:n.382G=
NM_001302961.1:c.85G= NP_001289890.1:p.Glu29=
NM_004917.4:c.370G= NP_004908.4:p.Glu124=
NR_126566.1:n.363G=
XM_005259441.3:c.85G= XP_005259498.2:p.Glu29=
XM_011527545.1:c.370G= XP_011525847.1:p.Glu124=
XM_011527546.1:c.370G= XP_011525848.1:p.Glu124=
XM_011527547.1:c.223G= XP_011525849.1:p.Glu75=
XM_005259441.4:c.85G= XP_005259498.2:p.Glu29=
XM_011527545.3:c.370G= XP_011525847.1:p.Glu124=
XM_011527546.2:c.370G= XP_011525848.1:p.Glu124=
NM_001302961.2:c.85G= NP_001289890.1:p.Glu29=
NR_126566.2:n.363G=
NM_004917.5:c.370G= MANE Select NP_004908.4:p.Glu124=