Canonical Allele Identifier: CA407041188

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411747T>A (hg19) ; chr19:g.50908491T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908491T>A , CM000681.2:g.50908491T>A	GRCh38
NC_000019.9:g.51411747T>A , CM000681.1:g.51411747T>A	GRCh37
NC_000019.8:g.56103559T>A	NCBI36
NG_012154.2:g.7248A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.480A>T MANE Select	ENSP00000326159.1:p.Arg160Ser
ENST00000324041.5:c.480A>T	ENSP00000326159.1:p.Arg160Ser
ENST00000431178.2:c.328+88A>T	ENSP00000399448.2:n.328+88A>T
ENST00000593885.1:c.191A>T	ENSP00000469769.1:p.Glu64Val
ENST00000596876.1:n.482A>T
ENST00000598305.5:c.191A>T	ENSP00000469963.1:p.Glu64Val
ENST00000599865.5:n.416A>T
ENST00000602148.1:c.492A>T	ENSP00000472091.1:n.492A>T
NM_001302961.1:c.195A>T	NP_001289890.1:p.Arg65Ser
NM_004917.4:c.480A>T	NP_004908.4:p.Arg160Ser
NR_126566.1:n.469A>T
XM_005259441.3:c.195A>T	XP_005259498.2:p.Arg65Ser
XM_011527545.1:c.476A>T	XP_011525847.1:p.Glu159Val
XM_011527546.1:c.475+88A>T	XP_011525848.1:n.475+88A>T
XM_011527547.1:c.333A>T	XP_011525849.1:p.Arg111Ser
XM_005259441.4:c.195A>T	XP_005259498.2:p.Arg65Ser
XM_011527545.3:c.476A>T	XP_011525847.1:p.Glu159Val
XM_011527546.2:c.475+88A>T	XP_011525848.1:n.475+88A>T
NM_001302961.2:c.195A>T	NP_001289890.1:p.Arg65Ser
NR_126566.2:n.469A>T
NM_004917.5:c.480A>T MANE Select	NP_004908.4:p.Arg160Ser