Canonical Allele Identifier: CA407041605
Gene: KLK4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908700C>T , CM000681.2:g.50908700C>T GRCh38
NC_000019.9:g.51411956C>T , CM000681.1:g.51411956C>T GRCh37
NC_000019.8:g.56103768C>T NCBI36
NG_012154.2:g.7039G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000324041.6:c.354G>A MANE Select ENSP00000326159.1:p.Met118Ile
ENST00000324041.5:c.354G>A ENSP00000326159.1:p.Met118Ile
ENST00000431178.2:c.207G>A ENSP00000399448.2:p.Met69Ile
ENST00000593885.1:c.69G>A ENSP00000469769.1:p.Met23Ile
ENST00000596876.1:n.273G>A
ENST00000598305.5:c.69G>A ENSP00000469963.1:p.Met23Ile
ENST00000599865.5:n.207G>A
ENST00000602148.1:c.366G>A ENSP00000472091.1:n.366G>A
NM_001302961.1:c.69G>A NP_001289890.1:p.Met23Ile
NM_004917.4:c.354G>A NP_004908.4:p.Met118Ile
NR_126566.1:n.347G>A
XM_005259441.3:c.69G>A XP_005259498.2:p.Met23Ile
XM_011527545.1:c.354G>A XP_011525847.1:p.Met118Ile
XM_011527546.1:c.354G>A XP_011525848.1:p.Met118Ile
XM_011527547.1:c.207G>A XP_011525849.1:p.Met69Ile
XM_005259441.4:c.69G>A XP_005259498.2:p.Met23Ile
XM_011527545.3:c.354G>A XP_011525847.1:p.Met118Ile
XM_011527546.2:c.354G>A XP_011525848.1:p.Met118Ile
NM_001302961.2:c.69G>A NP_001289890.1:p.Met23Ile
NR_126566.2:n.347G>A
NM_004917.5:c.354G>A MANE Select NP_004908.4:p.Met118Ile