Canonical Allele Identifier: CA309662018

Gene: KLK4

Linked Data

• dbSNP Id: rs890552229
• gnomAD v2: 19-51411725-C-T
• gnomAD v4: 19-50908469-C-T
• MyVariant Identifiers: chr19:g.51411725C>T (hg19) ; chr19:g.50908469C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908469C>T , CM000681.2:g.50908469C>T	GRCh38
NC_000019.9:g.51411725C>T , CM000681.1:g.51411725C>T	GRCh37
NC_000019.8:g.56103537C>T	NCBI36
NG_012154.2:g.7270G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.502G>A MANE Select	ENSP00000326159.1:p.Val168Met
ENST00000324041.5:c.502G>A	ENSP00000326159.1:p.Val168Met
ENST00000431178.2:c.328+110G>A	ENSP00000399448.2:n.328+110G>A
ENST00000593885.1:c.213G>A	ENSP00000469769.1:p.Ala71=
ENST00000596876.1:n.504G>A
ENST00000598305.5:c.213G>A	ENSP00000469963.1:p.Ala71=
ENST00000599865.5:n.438G>A
ENST00000602148.1:c.514G>A	ENSP00000472091.1:n.514G>A
NM_001302961.1:c.217G>A	NP_001289890.1:p.Val73Met
NM_004917.4:c.502G>A	NP_004908.4:p.Val168Met
NR_126566.1:n.491G>A
XM_005259441.3:c.217G>A	XP_005259498.2:p.Val73Met
XM_011527545.1:c.498G>A	XP_011525847.1:p.Ala166=
XM_011527546.1:c.475+110G>A	XP_011525848.1:n.475+110G>A
XM_011527547.1:c.355G>A	XP_011525849.1:p.Val119Met
XM_005259441.4:c.217G>A	XP_005259498.2:p.Val73Met
XM_011527545.3:c.498G>A	XP_011525847.1:p.Ala166=
XM_011527546.2:c.475+110G>A	XP_011525848.1:n.475+110G>A
NM_001302961.2:c.217G>A	NP_001289890.1:p.Val73Met
NR_126566.2:n.491G>A
NM_004917.5:c.502G>A MANE Select	NP_004908.4:p.Val168Met