Canonical Allele Identifier: CA407040636

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411685A>T (hg19) ; chr19:g.50908429A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908429A>T , CM000681.2:g.50908429A>T	GRCh38
NC_000019.9:g.51411685A>T , CM000681.1:g.51411685A>T	GRCh37
NC_000019.8:g.56103497A>T	NCBI36
NG_012154.2:g.7310T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.542T>A MANE Select	ENSP00000326159.1:p.Leu181His
ENST00000324041.5:c.542T>A	ENSP00000326159.1:p.Leu181His
ENST00000431178.2:c.328+150T>A	ENSP00000399448.2:n.328+150T>A
ENST00000593885.1:c.*37T>A	ENSP00000469769.1:n.*37T>A
ENST00000596876.1:n.544T>A
ENST00000598305.5:c.*37T>A	ENSP00000469963.1:n.*37T>A
ENST00000599865.5:n.478T>A
ENST00000602148.1:c.554T>A	ENSP00000472091.1:n.554T>A
NM_001302961.1:c.257T>A	NP_001289890.1:p.Leu86His
NM_004917.4:c.542T>A	NP_004908.4:p.Leu181His
NR_126566.1:n.531T>A
XM_005259441.3:c.257T>A	XP_005259498.2:p.Leu86His
XM_011527545.1:c.*37T>A	XP_011525847.1:n.*37T>A
XM_011527546.1:c.475+150T>A	XP_011525848.1:n.475+150T>A
XM_011527547.1:c.395T>A	XP_011525849.1:p.Leu132His
XM_005259441.4:c.257T>A	XP_005259498.2:p.Leu86His
XM_011527545.3:c.*37T>A	XP_011525847.1:n.*37T>A
XM_011527546.2:c.475+150T>A	XP_011525848.1:n.475+150T>A
NM_001302961.2:c.257T>A	NP_001289890.1:p.Leu86His
NR_126566.2:n.531T>A
NM_004917.5:c.542T>A MANE Select	NP_004908.4:p.Leu181His