Canonical Allele Identifier: CA508313895

Gene: KLK4

Linked Data

• dbSNP Id: rs2090455414
• gnomAD v4: 19-50908607-G-A
• COSMIC: COSM375317
• MyVariant Identifiers: chr19:g.51411863G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908607G>A , CM000681.2:g.50908607G>A	GRCh38
NC_000019.9:g.51411863G>A , CM000681.1:g.51411863G>A	GRCh37
NC_000019.8:g.56103675G>A	NCBI36
NG_012154.2:g.7132C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000324041.6:c.447C>T MANE Select	ENSP00000326159.1:p.Leu149=
ENST00000324041.5:c.447C>T	ENSP00000326159.1:p.Leu149=
ENST00000431178.2:c.300C>T	ENSP00000399448.2:p.Leu100=
ENST00000593885.1:c.162C>T	ENSP00000469769.1:p.Leu54=
ENST00000596876.1:n.366C>T
ENST00000598305.5:c.162C>T	ENSP00000469963.1:p.Leu54=
ENST00000599865.5:n.300C>T
ENST00000602148.1:c.459C>T	ENSP00000472091.1:n.459C>T
NM_001302961.1:c.162C>T	NP_001289890.1:p.Leu54=
NM_004917.4:c.447C>T	NP_004908.4:p.Leu149=
NR_126566.1:n.440C>T
XM_005259441.3:c.162C>T	XP_005259498.2:p.Leu54=
XM_011527545.1:c.447C>T	XP_011525847.1:p.Leu149=
XM_011527546.1:c.447C>T	XP_011525848.1:p.Leu149=
XM_011527547.1:c.300C>T	XP_011525849.1:p.Leu100=
XM_005259441.4:c.162C>T	XP_005259498.2:p.Leu54=
XM_011527545.3:c.447C>T	XP_011525847.1:p.Leu149=
XM_011527546.2:c.447C>T	XP_011525848.1:p.Leu149=
NM_001302961.2:c.162C>T	NP_001289890.1:p.Leu54=
NR_126566.2:n.440C>T
NM_004917.5:c.447C>T MANE Select	NP_004908.4:p.Leu149=