Canonical Allele Identifier: CA2341138340
Gene: KLK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908556C= , CM000681.2:g.50908556C= GRCh38
NC_000019.9:g.51411812C= , CM000681.1:g.51411812C= GRCh37
NC_000019.8:g.56103624C= NCBI36
NG_012154.2:g.7183G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000324041.6:c.475+23G= MANE Select ENSP00000326159.1:n.475+23G=
ENST00000324041.5:c.475+23G= ENSP00000326159.1:n.475+23G=
ENST00000431178.2:c.328+23G= ENSP00000399448.2:n.328+23G=
ENST00000593885.1:c.190+23G= ENSP00000469769.1:n.190+23G=
ENST00000596876.1:n.417G=
ENST00000598305.5:c.190+23G= ENSP00000469963.1:n.190+23G=
ENST00000599865.5:n.351G=
ENST00000602148.1:c.487+23G= ENSP00000472091.1:n.487+23G=
NM_001302961.1:c.190+23G= NP_001289890.1:n.190+23G=
NM_004917.4:c.475+23G= NP_004908.4:n.475+23G=
NR_126566.1:n.468+23G=
XM_005259441.3:c.190+23G= XP_005259498.2:n.190+23G=
XM_011527545.1:c.475+23G= XP_011525847.1:n.475+23G=
XM_011527546.1:c.475+23G= XP_011525848.1:n.475+23G=
XM_011527547.1:c.328+23G= XP_011525849.1:n.328+23G=
XM_005259441.4:c.190+23G= XP_005259498.2:n.190+23G=
XM_011527545.3:c.475+23G= XP_011525847.1:n.475+23G=
XM_011527546.2:c.475+23G= XP_011525848.1:n.475+23G=
NM_001302961.2:c.190+23G= NP_001289890.1:n.190+23G=
NR_126566.2:n.468+23G=
NM_004917.5:c.475+23G= MANE Select NP_004908.4:n.475+23G=