Canonical Allele Identifier: CA2341138274
Gene: KLK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908433T= , CM000681.2:g.50908433T= GRCh38
NC_000019.9:g.51411689T= , CM000681.1:g.51411689T= GRCh37
NC_000019.8:g.56103501T= NCBI36
NG_012154.2:g.7306A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000324041.6:c.538A= MANE Select ENSP00000326159.1:p.Lys180=
ENST00000324041.5:c.538A= ENSP00000326159.1:p.Lys180=
ENST00000431178.2:c.328+146A= ENSP00000399448.2:n.328+146A=
ENST00000593885.1:c.*33A= ENSP00000469769.1:n.*33A=
ENST00000596876.1:n.540A=
ENST00000598305.5:c.*33A= ENSP00000469963.1:n.*33A=
ENST00000599865.5:n.474A=
ENST00000602148.1:c.550A= ENSP00000472091.1:n.550A=
NM_001302961.1:c.253A= NP_001289890.1:p.Lys85=
NM_004917.4:c.538A= NP_004908.4:p.Lys180=
NR_126566.1:n.527A=
XM_005259441.3:c.253A= XP_005259498.2:p.Lys85=
XM_011527545.1:c.*33A= XP_011525847.1:n.*33A=
XM_011527546.1:c.475+146A= XP_011525848.1:n.475+146A=
XM_011527547.1:c.391A= XP_011525849.1:p.Lys131=
XM_005259441.4:c.253A= XP_005259498.2:p.Lys85=
XM_011527545.3:c.*33A= XP_011525847.1:n.*33A=
XM_011527546.2:c.475+146A= XP_011525848.1:n.475+146A=
NM_001302961.2:c.253A= NP_001289890.1:p.Lys85=
NR_126566.2:n.527A=
NM_004917.5:c.538A= MANE Select NP_004908.4:p.Lys180=