Canonical Allele Identifier: CA407040624

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411682T>A (hg19) ; chr19:g.50908426T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908426T>A , CM000681.2:g.50908426T>A	GRCh38
NC_000019.9:g.51411682T>A , CM000681.1:g.51411682T>A	GRCh37
NC_000019.8:g.56103494T>A	NCBI36
NG_012154.2:g.7313A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.545A>T MANE Select	ENSP00000326159.1:p.Tyr182Phe
ENST00000324041.5:c.545A>T	ENSP00000326159.1:p.Tyr182Phe
ENST00000431178.2:c.328+153A>T	ENSP00000399448.2:n.328+153A>T
ENST00000593885.1:c.*40A>T	ENSP00000469769.1:n.*40A>T
ENST00000596876.1:n.547A>T
ENST00000598305.5:c.*40A>T	ENSP00000469963.1:n.*40A>T
ENST00000599865.5:n.481A>T
ENST00000602148.1:c.557A>T	ENSP00000472091.1:n.557A>T
NM_001302961.1:c.260A>T	NP_001289890.1:p.Tyr87Phe
NM_004917.4:c.545A>T	NP_004908.4:p.Tyr182Phe
NR_126566.1:n.534A>T
XM_005259441.3:c.260A>T	XP_005259498.2:p.Tyr87Phe
XM_011527545.1:c.*40A>T	XP_011525847.1:n.*40A>T
XM_011527546.1:c.475+153A>T	XP_011525848.1:n.475+153A>T
XM_011527547.1:c.398A>T	XP_011525849.1:p.Tyr133Phe
XM_005259441.4:c.260A>T	XP_005259498.2:p.Tyr87Phe
XM_011527545.3:c.*40A>T	XP_011525847.1:n.*40A>T
XM_011527546.2:c.475+153A>T	XP_011525848.1:n.475+153A>T
NM_001302961.2:c.260A>T	NP_001289890.1:p.Tyr87Phe
NR_126566.2:n.534A>T
NM_004917.5:c.545A>T MANE Select	NP_004908.4:p.Tyr182Phe