Canonical Allele Identifier: CA508313889

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411857A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908601A>G , CM000681.2:g.50908601A>G	GRCh38
NC_000019.9:g.51411857A>G , CM000681.1:g.51411857A>G	GRCh37
NC_000019.8:g.56103669A>G	NCBI36
NG_012154.2:g.7138T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000324041.6:c.453T>C MANE Select	ENSP00000326159.1:p.Ser151=
ENST00000324041.5:c.453T>C	ENSP00000326159.1:p.Ser151=
ENST00000431178.2:c.306T>C	ENSP00000399448.2:p.Ser102=
ENST00000593885.1:c.168T>C	ENSP00000469769.1:p.Ser56=
ENST00000596876.1:n.372T>C
ENST00000598305.5:c.168T>C	ENSP00000469963.1:p.Ser56=
ENST00000599865.5:n.306T>C
ENST00000602148.1:c.465T>C	ENSP00000472091.1:n.465T>C
NM_001302961.1:c.168T>C	NP_001289890.1:p.Ser56=
NM_004917.4:c.453T>C	NP_004908.4:p.Ser151=
NR_126566.1:n.446T>C
XM_005259441.3:c.168T>C	XP_005259498.2:p.Ser56=
XM_011527545.1:c.453T>C	XP_011525847.1:p.Ser151=
XM_011527546.1:c.453T>C	XP_011525848.1:p.Ser151=
XM_011527547.1:c.306T>C	XP_011525849.1:p.Ser102=
XM_005259441.4:c.168T>C	XP_005259498.2:p.Ser56=
XM_011527545.3:c.453T>C	XP_011525847.1:p.Ser151=
XM_011527546.2:c.453T>C	XP_011525848.1:p.Ser151=
NM_001302961.2:c.168T>C	NP_001289890.1:p.Ser56=
NR_126566.2:n.446T>C
NM_004917.5:c.453T>C MANE Select	NP_004908.4:p.Ser151=