Canonical Allele Identifier: CA407040526

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411666G>T (hg19) ; chr19:g.50908410G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.561C>A MANE Select	ENSP00000326159.1:p.His187Gln
ENST00000324041.5:c.561C>A	ENSP00000326159.1:p.His187Gln
ENST00000431178.2:c.328+169C>A	ENSP00000399448.2:n.328+169C>A
ENST00000593885.1:c.*56C>A	ENSP00000469769.1:n.*56C>A
ENST00000596876.1:n.563C>A
ENST00000598305.5:c.*56C>A	ENSP00000469963.1:n.*56C>A
ENST00000599865.5:n.497C>A
ENST00000602148.1:c.573C>A	ENSP00000472091.1:n.573C>A
NM_001302961.1:c.276C>A	NP_001289890.1:p.His92Gln
NM_004917.4:c.561C>A	NP_004908.4:p.His187Gln
NR_126566.1:n.550C>A
XM_005259441.3:c.276C>A	XP_005259498.2:p.His92Gln
XM_011527545.1:c.*56C>A	XP_011525847.1:n.*56C>A
XM_011527546.1:c.475+169C>A	XP_011525848.1:n.475+169C>A
XM_011527547.1:c.414C>A	XP_011525849.1:p.His138Gln
XM_005259441.4:c.276C>A	XP_005259498.2:p.His92Gln
XM_011527545.3:c.*56C>A	XP_011525847.1:n.*56C>A
XM_011527546.2:c.475+169C>A	XP_011525848.1:n.475+169C>A
NM_001302961.2:c.276C>A	NP_001289890.1:p.His92Gln
NR_126566.2:n.550C>A
NM_004917.5:c.561C>A MANE Select	NP_004908.4:p.His187Gln