Canonical Allele Identifier: CA2341138285
Gene: KLK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908459G= , CM000681.2:g.50908459G= GRCh38
NC_000019.9:g.51411715G= , CM000681.1:g.51411715G= GRCh37
NC_000019.8:g.56103527G= NCBI36
NG_012154.2:g.7280C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000324041.6:c.512C= MANE Select ENSP00000326159.1:p.Ser171=
ENST00000324041.5:c.512C= ENSP00000326159.1:p.Ser171=
ENST00000431178.2:c.328+120C= ENSP00000399448.2:n.328+120C=
ENST00000593885.1:c.*7C= ENSP00000469769.1:n.*7C=
ENST00000596876.1:n.514C=
ENST00000598305.5:c.*7C= ENSP00000469963.1:n.*7C=
ENST00000599865.5:n.448C=
ENST00000602148.1:c.524C= ENSP00000472091.1:n.524C=
NM_001302961.1:c.227C= NP_001289890.1:p.Ser76=
NM_004917.4:c.512C= NP_004908.4:p.Ser171=
NR_126566.1:n.501C=
XM_005259441.3:c.227C= XP_005259498.2:p.Ser76=
XM_011527545.1:c.*7C= XP_011525847.1:n.*7C=
XM_011527546.1:c.475+120C= XP_011525848.1:n.475+120C=
XM_011527547.1:c.365C= XP_011525849.1:p.Ser122=
XM_005259441.4:c.227C= XP_005259498.2:p.Ser76=
XM_011527545.3:c.*7C= XP_011525847.1:n.*7C=
XM_011527546.2:c.475+120C= XP_011525848.1:n.475+120C=
NM_001302961.2:c.227C= NP_001289890.1:p.Ser76=
NR_126566.2:n.501C=
NM_004917.5:c.512C= MANE Select NP_004908.4:p.Ser171=