Canonical Allele Identifier: CA9605096

Gene: KLK4

Linked Data

• ClinVar Variation Id: 782657
• ClinVar RCV Id: RCV000964076
• dbSNP Id: rs198966
• ExAC: 19:51412010 G / A
• gnomAD v2: 19-51412010-G-A
• gnomAD v3: 19-50908754-G-A
• gnomAD v4: 19-50908754-G-A
• MyVariant Identifiers: chr19:g.51412010G>A (hg19) ; chr19:g.50908754G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908754G>A , CM000681.2:g.50908754G>A	GRCh38
NC_000019.9:g.51412010G>A , CM000681.1:g.51412010G>A	GRCh37
NC_000019.8:g.56103822G>A	NCBI36
NG_012154.2:g.6985C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.300C>T MANE Select	ENSP00000326159.1:p.Ser100=
ENST00000324041.5:c.300C>T	ENSP00000326159.1:p.Ser100=
ENST00000431178.2:c.153C>T	ENSP00000399448.2:p.Ser51=
ENST00000593885.1:c.15C>T	ENSP00000469769.1:p.Ser5=
ENST00000596876.1:n.219C>T
ENST00000598305.5:c.15C>T	ENSP00000469963.1:p.Ser5=
ENST00000599865.5:n.153C>T
ENST00000602148.1:c.312C>T	ENSP00000472091.1:n.312C>T
NM_001302961.1:c.15C>T	NP_001289890.1:p.Ser5=
NM_004917.4:c.300C>T	NP_004908.4:p.Ser100=
NR_126566.1:n.293C>T
XM_005259441.3:c.15C>T	XP_005259498.2:p.Ser5=
XM_011527545.1:c.300C>T	XP_011525847.1:p.Ser100=
XM_011527546.1:c.300C>T	XP_011525848.1:p.Ser100=
XM_011527547.1:c.153C>T	XP_011525849.1:p.Ser51=
XM_005259441.4:c.15C>T	XP_005259498.2:p.Ser5=
XM_011527545.3:c.300C>T	XP_011525847.1:p.Ser100=
XM_011527546.2:c.300C>T	XP_011525848.1:p.Ser100=
NM_001302961.2:c.15C>T	NP_001289890.1:p.Ser5=
NR_126566.2:n.293C>T
NM_004917.5:c.300C>T MANE Select	NP_004908.4:p.Ser100=