Canonical Allele Identifier: CA407041175
Gene: KLK4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908486G>T , CM000681.2:g.50908486G>T GRCh38
NC_000019.9:g.51411742G>T , CM000681.1:g.51411742G>T GRCh37
NC_000019.8:g.56103554G>T NCBI36
NG_012154.2:g.7253C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000324041.6:c.485C>A MANE Select ENSP00000326159.1:p.Pro162His
ENST00000324041.5:c.485C>A ENSP00000326159.1:p.Pro162His
ENST00000431178.2:c.328+93C>A ENSP00000399448.2:n.328+93C>A
ENST00000593885.1:c.196C>A ENSP00000469769.1:p.Leu66Ile
ENST00000596876.1:n.487C>A
ENST00000598305.5:c.196C>A ENSP00000469963.1:p.Leu66Ile
ENST00000599865.5:n.421C>A
ENST00000602148.1:c.497C>A ENSP00000472091.1:n.497C>A
NM_001302961.1:c.200C>A NP_001289890.1:p.Pro67His
NM_004917.4:c.485C>A NP_004908.4:p.Pro162His
NR_126566.1:n.474C>A
XM_005259441.3:c.200C>A XP_005259498.2:p.Pro67His
XM_011527545.1:c.481C>A XP_011525847.1:p.Leu161Ile
XM_011527546.1:c.475+93C>A XP_011525848.1:n.475+93C>A
XM_011527547.1:c.338C>A XP_011525849.1:p.Pro113His
XM_005259441.4:c.200C>A XP_005259498.2:p.Pro67His
XM_011527545.3:c.481C>A XP_011525847.1:p.Leu161Ile
XM_011527546.2:c.475+93C>A XP_011525848.1:n.475+93C>A
NM_001302961.2:c.200C>A NP_001289890.1:p.Pro67His
NR_126566.2:n.474C>A
NM_004917.5:c.485C>A MANE Select NP_004908.4:p.Pro162His