Canonical Allele Identifier: CA117930
Gene: KLK4 HGNC NCBI

Linked Data

ClinVar Variation Id: 6079
ClinVar RCV Id: RCV000006452
dbSNP Id: rs104894704

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908596C>T , CM000681.2:g.50908596C>T GRCh38
NC_000019.9:g.51411852C>T , CM000681.1:g.51411852C>T GRCh37
NC_000019.8:g.56103664C>T NCBI36
NG_012154.2:g.7143G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000324041.6:c.458G>A MANE Select ENSP00000326159.1:p.Trp153Ter
ENST00000324041.5:c.458G>A ENSP00000326159.1:p.Trp153Ter
ENST00000431178.2:c.311G>A ENSP00000399448.2:p.Trp104Ter
ENST00000593885.1:c.173G>A ENSP00000469769.1:p.Trp58Ter
ENST00000596876.1:n.377G>A
ENST00000598305.5:c.173G>A ENSP00000469963.1:p.Trp58Ter
ENST00000599865.5:n.311G>A
ENST00000602148.1:c.470G>A ENSP00000472091.1:n.470G>A
NM_001302961.1:c.173G>A NP_001289890.1:p.Trp58Ter
NM_004917.4:c.458G>A NP_004908.4:p.Trp153Ter
NR_126566.1:n.451G>A
XM_005259441.3:c.173G>A XP_005259498.2:p.Trp58Ter
XM_011527545.1:c.458G>A XP_011525847.1:p.Trp153Ter
XM_011527546.1:c.458G>A XP_011525848.1:p.Trp153Ter
XM_011527547.1:c.311G>A XP_011525849.1:p.Trp104Ter
XM_005259441.4:c.173G>A XP_005259498.2:p.Trp58Ter
XM_011527545.3:c.458G>A XP_011525847.1:p.Trp153Ter
XM_011527546.2:c.458G>A XP_011525848.1:p.Trp153Ter
NM_001302961.2:c.173G>A NP_001289890.1:p.Trp58Ter
NR_126566.2:n.451G>A
NM_004917.5:c.458G>A MANE Select NP_004908.4:p.Trp153Ter