Canonical Allele Identifier: CA508313957
Gene: KLK4 HGNC NCBI

Linked Data

dbSNP Id: rs1437908996

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908670C>T , CM000681.2:g.50908670C>T GRCh38
NC_000019.9:g.51411926C>T , CM000681.1:g.51411926C>T GRCh37
NC_000019.8:g.56103738C>T NCBI36
NG_012154.2:g.7069G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000324041.6:c.384G>A MANE Select ENSP00000326159.1:p.Glu128=
ENST00000324041.5:c.384G>A ENSP00000326159.1:p.Glu128=
ENST00000431178.2:c.237G>A ENSP00000399448.2:p.Glu79=
ENST00000593885.1:c.99G>A ENSP00000469769.1:p.Glu33=
ENST00000596876.1:n.303G>A
ENST00000598305.5:c.99G>A ENSP00000469963.1:p.Glu33=
ENST00000599865.5:n.237G>A
ENST00000602148.1:c.396G>A ENSP00000472091.1:n.396G>A
NM_001302961.1:c.99G>A NP_001289890.1:p.Glu33=
NM_004917.4:c.384G>A NP_004908.4:p.Glu128=
NR_126566.1:n.377G>A
XM_005259441.3:c.99G>A XP_005259498.2:p.Glu33=
XM_011527545.1:c.384G>A XP_011525847.1:p.Glu128=
XM_011527546.1:c.384G>A XP_011525848.1:p.Glu128=
XM_011527547.1:c.237G>A XP_011525849.1:p.Glu79=
XM_005259441.4:c.99G>A XP_005259498.2:p.Glu33=
XM_011527545.3:c.384G>A XP_011525847.1:p.Glu128=
XM_011527546.2:c.384G>A XP_011525848.1:p.Glu128=
NM_001302961.2:c.99G>A NP_001289890.1:p.Glu33=
NR_126566.2:n.377G>A
NM_004917.5:c.384G>A MANE Select NP_004908.4:p.Glu128=