Canonical Allele Identifier: CA508313840

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411735C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908479C>T , CM000681.2:g.50908479C>T	GRCh38
NC_000019.9:g.51411735C>T , CM000681.1:g.51411735C>T	GRCh37
NC_000019.8:g.56103547C>T	NCBI36
NG_012154.2:g.7260G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.492G>A MANE Select	ENSP00000326159.1:p.Val164=
ENST00000324041.5:c.492G>A	ENSP00000326159.1:p.Val164=
ENST00000431178.2:c.328+100G>A	ENSP00000399448.2:n.328+100G>A
ENST00000593885.1:c.203G>A	ENSP00000469769.1:p.Cys68Tyr
ENST00000596876.1:n.494G>A
ENST00000598305.5:c.203G>A	ENSP00000469963.1:p.Cys68Tyr
ENST00000599865.5:n.428G>A
ENST00000602148.1:c.504G>A	ENSP00000472091.1:n.504G>A
NM_001302961.1:c.207G>A	NP_001289890.1:p.Val69=
NM_004917.4:c.492G>A	NP_004908.4:p.Val164=
NR_126566.1:n.481G>A
XM_005259441.3:c.207G>A	XP_005259498.2:p.Val69=
XM_011527545.1:c.488G>A	XP_011525847.1:p.Cys163Tyr
XM_011527546.1:c.475+100G>A	XP_011525848.1:n.475+100G>A
XM_011527547.1:c.345G>A	XP_011525849.1:p.Val115=
XM_005259441.4:c.207G>A	XP_005259498.2:p.Val69=
XM_011527545.3:c.488G>A	XP_011525847.1:p.Cys163Tyr
XM_011527546.2:c.475+100G>A	XP_011525848.1:n.475+100G>A
NM_001302961.2:c.207G>A	NP_001289890.1:p.Val69=
NR_126566.2:n.481G>A
NM_004917.5:c.492G>A MANE Select	NP_004908.4:p.Val164=