Canonical Allele Identifier: CA508211900

Gene: KLK4

Linked Data

• dbSNP Id: rs2090452872
• gnomAD v4: 19-50908410-G-A
• MyVariant Identifiers: chr19:g.51411666G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908410G>A , CM000681.2:g.50908410G>A	GRCh38
NC_000019.9:g.51411666G>A , CM000681.1:g.51411666G>A	GRCh37
NC_000019.8:g.56103478G>A	NCBI36
NG_012154.2:g.7329C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.561C>T MANE Select	ENSP00000326159.1:p.His187=
ENST00000324041.5:c.561C>T	ENSP00000326159.1:p.His187=
ENST00000431178.2:c.328+169C>T	ENSP00000399448.2:n.328+169C>T
ENST00000593885.1:c.*56C>T	ENSP00000469769.1:n.*56C>T
ENST00000596876.1:n.563C>T
ENST00000598305.5:c.*56C>T	ENSP00000469963.1:n.*56C>T
ENST00000599865.5:n.497C>T
ENST00000602148.1:c.573C>T	ENSP00000472091.1:n.573C>T
NM_001302961.1:c.276C>T	NP_001289890.1:p.His92=
NM_004917.4:c.561C>T	NP_004908.4:p.His187=
NR_126566.1:n.550C>T
XM_005259441.3:c.276C>T	XP_005259498.2:p.His92=
XM_011527545.1:c.*56C>T	XP_011525847.1:n.*56C>T
XM_011527546.1:c.475+169C>T	XP_011525848.1:n.475+169C>T
XM_011527547.1:c.414C>T	XP_011525849.1:p.His138=
XM_005259441.4:c.276C>T	XP_005259498.2:p.His92=
XM_011527545.3:c.*56C>T	XP_011525847.1:n.*56C>T
XM_011527546.2:c.475+169C>T	XP_011525848.1:n.475+169C>T
NM_001302961.2:c.276C>T	NP_001289890.1:p.His92=
NR_126566.2:n.550C>T
NM_004917.5:c.561C>T MANE Select	NP_004908.4:p.His187=