Canonical Allele Identifier: CA508212128

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411717C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908461C>G , CM000681.2:g.50908461C>G	GRCh38
NC_000019.9:g.51411717C>G , CM000681.1:g.51411717C>G	GRCh37
NC_000019.8:g.56103529C>G	NCBI36
NG_012154.2:g.7278G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.510G>C MANE Select	ENSP00000326159.1:p.Val170=
ENST00000324041.5:c.510G>C	ENSP00000326159.1:p.Val170=
ENST00000431178.2:c.328+118G>C	ENSP00000399448.2:n.328+118G>C
ENST00000593885.1:c.*5G>C	ENSP00000469769.1:n.*5G>C
ENST00000596876.1:n.512G>C
ENST00000598305.5:c.*5G>C	ENSP00000469963.1:n.*5G>C
ENST00000599865.5:n.446G>C
ENST00000602148.1:c.522G>C	ENSP00000472091.1:n.522G>C
NM_001302961.1:c.225G>C	NP_001289890.1:p.Val75=
NM_004917.4:c.510G>C	NP_004908.4:p.Val170=
NR_126566.1:n.499G>C
XM_005259441.3:c.225G>C	XP_005259498.2:p.Val75=
XM_011527545.1:c.*5G>C	XP_011525847.1:n.*5G>C
XM_011527546.1:c.475+118G>C	XP_011525848.1:n.475+118G>C
XM_011527547.1:c.363G>C	XP_011525849.1:p.Val121=
XM_005259441.4:c.225G>C	XP_005259498.2:p.Val75=
XM_011527545.3:c.*5G>C	XP_011525847.1:n.*5G>C
XM_011527546.2:c.475+118G>C	XP_011525848.1:n.475+118G>C
NM_001302961.2:c.225G>C	NP_001289890.1:p.Val75=
NR_126566.2:n.499G>C
NM_004917.5:c.510G>C MANE Select	NP_004908.4:p.Val170=