Canonical Allele Identifier: CA407040586

Gene: KLK4

Linked Data

• gnomAD v4: 19-50908420-G-A
• MyVariant Identifiers: chr19:g.51411676G>A (hg19) ; chr19:g.50908420G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908420G>A , CM000681.2:g.50908420G>A	GRCh38
NC_000019.9:g.51411676G>A , CM000681.1:g.51411676G>A	GRCh37
NC_000019.8:g.56103488G>A	NCBI36
NG_012154.2:g.7319C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.551C>T MANE Select	ENSP00000326159.1:p.Pro184Leu
ENST00000324041.5:c.551C>T	ENSP00000326159.1:p.Pro184Leu
ENST00000431178.2:c.328+159C>T	ENSP00000399448.2:n.328+159C>T
ENST00000593885.1:c.*46C>T	ENSP00000469769.1:n.*46C>T
ENST00000596876.1:n.553C>T
ENST00000598305.5:c.*46C>T	ENSP00000469963.1:n.*46C>T
ENST00000599865.5:n.487C>T
ENST00000602148.1:c.563C>T	ENSP00000472091.1:n.563C>T
NM_001302961.1:c.266C>T	NP_001289890.1:p.Pro89Leu
NM_004917.4:c.551C>T	NP_004908.4:p.Pro184Leu
NR_126566.1:n.540C>T
XM_005259441.3:c.266C>T	XP_005259498.2:p.Pro89Leu
XM_011527545.1:c.*46C>T	XP_011525847.1:n.*46C>T
XM_011527546.1:c.475+159C>T	XP_011525848.1:n.475+159C>T
XM_011527547.1:c.404C>T	XP_011525849.1:p.Pro135Leu
XM_005259441.4:c.266C>T	XP_005259498.2:p.Pro89Leu
XM_011527545.3:c.*46C>T	XP_011525847.1:n.*46C>T
XM_011527546.2:c.475+159C>T	XP_011525848.1:n.475+159C>T
NM_001302961.2:c.266C>T	NP_001289890.1:p.Pro89Leu
NR_126566.2:n.540C>T
NM_004917.5:c.551C>T MANE Select	NP_004908.4:p.Pro184Leu