Canonical Allele Identifier: CA407041355

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411868A>G (hg19) ; chr19:g.50908612A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908612A>G , CM000681.2:g.50908612A>G	GRCh38
NC_000019.9:g.51411868A>G , CM000681.1:g.51411868A>G	GRCh37
NC_000019.8:g.56103680A>G	NCBI36
NG_012154.2:g.7127T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.442T>C MANE Select	ENSP00000326159.1:p.Cys148Arg
ENST00000324041.5:c.442T>C	ENSP00000326159.1:p.Cys148Arg
ENST00000431178.2:c.295T>C	ENSP00000399448.2:p.Cys99Arg
ENST00000593885.1:c.157T>C	ENSP00000469769.1:p.Cys53Arg
ENST00000596876.1:n.361T>C
ENST00000598305.5:c.157T>C	ENSP00000469963.1:p.Cys53Arg
ENST00000599865.5:n.295T>C
ENST00000602148.1:c.454T>C	ENSP00000472091.1:n.454T>C
NM_001302961.1:c.157T>C	NP_001289890.1:p.Cys53Arg
NM_004917.4:c.442T>C	NP_004908.4:p.Cys148Arg
NR_126566.1:n.435T>C
XM_005259441.3:c.157T>C	XP_005259498.2:p.Cys53Arg
XM_011527545.1:c.442T>C	XP_011525847.1:p.Cys148Arg
XM_011527546.1:c.442T>C	XP_011525848.1:p.Cys148Arg
XM_011527547.1:c.295T>C	XP_011525849.1:p.Cys99Arg
XM_005259441.4:c.157T>C	XP_005259498.2:p.Cys53Arg
XM_011527545.3:c.442T>C	XP_011525847.1:p.Cys148Arg
XM_011527546.2:c.442T>C	XP_011525848.1:p.Cys148Arg
NM_001302961.2:c.157T>C	NP_001289890.1:p.Cys53Arg
NR_126566.2:n.435T>C
NM_004917.5:c.442T>C MANE Select	NP_004908.4:p.Cys148Arg