Canonical Allele Identifier: CA508313834

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411732C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908476C>A , CM000681.2:g.50908476C>A	GRCh38
NC_000019.9:g.51411732C>A , CM000681.1:g.51411732C>A	GRCh37
NC_000019.8:g.56103544C>A	NCBI36
NG_012154.2:g.7263G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.495G>T MANE Select	ENSP00000326159.1:p.Leu165=
ENST00000324041.5:c.495G>T	ENSP00000326159.1:p.Leu165=
ENST00000431178.2:c.328+103G>T	ENSP00000399448.2:n.328+103G>T
ENST00000593885.1:c.206G>T	ENSP00000469769.1:p.Cys69Phe
ENST00000596876.1:n.497G>T
ENST00000598305.5:c.206G>T	ENSP00000469963.1:p.Cys69Phe
ENST00000599865.5:n.431G>T
ENST00000602148.1:c.507G>T	ENSP00000472091.1:n.507G>T
NM_001302961.1:c.210G>T	NP_001289890.1:p.Leu70=
NM_004917.4:c.495G>T	NP_004908.4:p.Leu165=
NR_126566.1:n.484G>T
XM_005259441.3:c.210G>T	XP_005259498.2:p.Leu70=
XM_011527545.1:c.491G>T	XP_011525847.1:p.Cys164Phe
XM_011527546.1:c.475+103G>T	XP_011525848.1:n.475+103G>T
XM_011527547.1:c.348G>T	XP_011525849.1:p.Leu116=
XM_005259441.4:c.210G>T	XP_005259498.2:p.Leu70=
XM_011527545.3:c.491G>T	XP_011525847.1:p.Cys164Phe
XM_011527546.2:c.475+103G>T	XP_011525848.1:n.475+103G>T
NM_001302961.2:c.210G>T	NP_001289890.1:p.Leu70=
NR_126566.2:n.484G>T
NM_004917.5:c.495G>T MANE Select	NP_004908.4:p.Leu165=