Canonical Allele Identifier: CA309662093

Gene: KLK4

Linked Data

• dbSNP Id: rs970897746
• gnomAD v4: 19-50908606-C-T
• COSMIC: COSM1395577
• MyVariant Identifiers: chr19:g.51411862C>T (hg19) ; chr19:g.50908606C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908606C>T , CM000681.2:g.50908606C>T	GRCh38
NC_000019.9:g.51411862C>T , CM000681.1:g.51411862C>T	GRCh37
NC_000019.8:g.56103674C>T	NCBI36
NG_012154.2:g.7133G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000324041.6:c.448G>A MANE Select	ENSP00000326159.1:p.Val150Ile
ENST00000324041.5:c.448G>A	ENSP00000326159.1:p.Val150Ile
ENST00000431178.2:c.301G>A	ENSP00000399448.2:p.Val101Ile
ENST00000593885.1:c.163G>A	ENSP00000469769.1:p.Val55Ile
ENST00000596876.1:n.367G>A
ENST00000598305.5:c.163G>A	ENSP00000469963.1:p.Val55Ile
ENST00000599865.5:n.301G>A
ENST00000602148.1:c.460G>A	ENSP00000472091.1:n.460G>A
NM_001302961.1:c.163G>A	NP_001289890.1:p.Val55Ile
NM_004917.4:c.448G>A	NP_004908.4:p.Val150Ile
NR_126566.1:n.441G>A
XM_005259441.3:c.163G>A	XP_005259498.2:p.Val55Ile
XM_011527545.1:c.448G>A	XP_011525847.1:p.Val150Ile
XM_011527546.1:c.448G>A	XP_011525848.1:p.Val150Ile
XM_011527547.1:c.301G>A	XP_011525849.1:p.Val101Ile
XM_005259441.4:c.163G>A	XP_005259498.2:p.Val55Ile
XM_011527545.3:c.448G>A	XP_011525847.1:p.Val150Ile
XM_011527546.2:c.448G>A	XP_011525848.1:p.Val150Ile
NM_001302961.2:c.163G>A	NP_001289890.1:p.Val55Ile
NR_126566.2:n.441G>A
NM_004917.5:c.448G>A MANE Select	NP_004908.4:p.Val150Ile