Canonical Allele Identifier: CA407041631
Gene: KLK4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908711T>A , CM000681.2:g.50908711T>A GRCh38
NC_000019.9:g.51411967T>A , CM000681.1:g.51411967T>A GRCh37
NC_000019.8:g.56103779T>A NCBI36
NG_012154.2:g.7028A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000324041.6:c.343A>T MANE Select ENSP00000326159.1:p.Asn115Tyr
ENST00000324041.5:c.343A>T ENSP00000326159.1:p.Asn115Tyr
ENST00000431178.2:c.196A>T ENSP00000399448.2:p.Asn66Tyr
ENST00000593885.1:c.58A>T ENSP00000469769.1:p.Asn20Tyr
ENST00000596876.1:n.262A>T
ENST00000598305.5:c.58A>T ENSP00000469963.1:p.Asn20Tyr
ENST00000599865.5:n.196A>T
ENST00000602148.1:c.355A>T ENSP00000472091.1:n.355A>T
NM_001302961.1:c.58A>T NP_001289890.1:p.Asn20Tyr
NM_004917.4:c.343A>T NP_004908.4:p.Asn115Tyr
NR_126566.1:n.336A>T
XM_005259441.3:c.58A>T XP_005259498.2:p.Asn20Tyr
XM_011527545.1:c.343A>T XP_011525847.1:p.Asn115Tyr
XM_011527546.1:c.343A>T XP_011525848.1:p.Asn115Tyr
XM_011527547.1:c.196A>T XP_011525849.1:p.Asn66Tyr
XM_005259441.4:c.58A>T XP_005259498.2:p.Asn20Tyr
XM_011527545.3:c.343A>T XP_011525847.1:p.Asn115Tyr
XM_011527546.2:c.343A>T XP_011525848.1:p.Asn115Tyr
NM_001302961.2:c.58A>T NP_001289890.1:p.Asn20Tyr
NR_126566.2:n.336A>T
NM_004917.5:c.343A>T MANE Select NP_004908.4:p.Asn115Tyr