Canonical Allele Identifier: CA407040425

Gene: KLK4

Linked Data

• gnomAD v4: 19-50908394-C-T
• MyVariant Identifiers: chr19:g.51411650C>T (hg19) ; chr19:g.50908394C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908394C>T , CM000681.2:g.50908394C>T	GRCh38
NC_000019.9:g.51411650C>T , CM000681.1:g.51411650C>T	GRCh37
NC_000019.8:g.56103462C>T	NCBI36
NG_012154.2:g.7345G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.577G>A MANE Select	ENSP00000326159.1:p.Ala193Thr
ENST00000324041.5:c.577G>A	ENSP00000326159.1:p.Ala193Thr
ENST00000431178.2:c.328+185G>A	ENSP00000399448.2:n.328+185G>A
ENST00000593885.1:c.*72G>A	ENSP00000469769.1:n.*72G>A
ENST00000596876.1:n.579G>A
ENST00000598305.5:c.*72G>A	ENSP00000469963.1:n.*72G>A
ENST00000599865.5:n.513G>A
ENST00000602148.1:c.589G>A	ENSP00000472091.1:n.589G>A
NM_001302961.1:c.292G>A	NP_001289890.1:p.Ala98Thr
NM_004917.4:c.577G>A	NP_004908.4:p.Ala193Thr
NR_126566.1:n.566G>A
XM_005259441.3:c.292G>A	XP_005259498.2:p.Ala98Thr
XM_011527545.1:c.*72G>A	XP_011525847.1:n.*72G>A
XM_011527546.1:c.475+185G>A	XP_011525848.1:n.475+185G>A
XM_011527547.1:c.430G>A	XP_011525849.1:p.Ala144Thr
XM_005259441.4:c.292G>A	XP_005259498.2:p.Ala98Thr
XM_011527545.3:c.*72G>A	XP_011525847.1:n.*72G>A
XM_011527546.2:c.475+185G>A	XP_011525848.1:n.475+185G>A
NM_001302961.2:c.292G>A	NP_001289890.1:p.Ala98Thr
NR_126566.2:n.566G>A
NM_004917.5:c.577G>A MANE Select	NP_004908.4:p.Ala193Thr