Canonical Allele Identifier: CA9605068

Gene: KLK4

Linked Data

• ClinVar Variation Id: 2340892
• ClinVar RCV Id: RCV002945043
• dbSNP Id: rs143632081
• ExAC: 19:51411867 C / T
• gnomAD v2: 19-51411867-C-T
• gnomAD v3: 19-50908611-C-T
• gnomAD v4: 19-50908611-C-T
• MyVariant Identifiers: chr19:g.51411867C>T (hg19) ; chr19:g.50908611C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908611C>T , CM000681.2:g.50908611C>T	GRCh38
NC_000019.9:g.51411867C>T , CM000681.1:g.51411867C>T	GRCh37
NC_000019.8:g.56103679C>T	NCBI36
NG_012154.2:g.7128G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.443G>A MANE Select	ENSP00000326159.1:p.Cys148Tyr
ENST00000324041.5:c.443G>A	ENSP00000326159.1:p.Cys148Tyr
ENST00000431178.2:c.296G>A	ENSP00000399448.2:p.Cys99Tyr
ENST00000593885.1:c.158G>A	ENSP00000469769.1:p.Cys53Tyr
ENST00000596876.1:n.362G>A
ENST00000598305.5:c.158G>A	ENSP00000469963.1:p.Cys53Tyr
ENST00000599865.5:n.296G>A
ENST00000602148.1:c.455G>A	ENSP00000472091.1:n.455G>A
NM_001302961.1:c.158G>A	NP_001289890.1:p.Cys53Tyr
NM_004917.4:c.443G>A	NP_004908.4:p.Cys148Tyr
NR_126566.1:n.436G>A
XM_005259441.3:c.158G>A	XP_005259498.2:p.Cys53Tyr
XM_011527545.1:c.443G>A	XP_011525847.1:p.Cys148Tyr
XM_011527546.1:c.443G>A	XP_011525848.1:p.Cys148Tyr
XM_011527547.1:c.296G>A	XP_011525849.1:p.Cys99Tyr
XM_005259441.4:c.158G>A	XP_005259498.2:p.Cys53Tyr
XM_011527545.3:c.443G>A	XP_011525847.1:p.Cys148Tyr
XM_011527546.2:c.443G>A	XP_011525848.1:p.Cys148Tyr
NM_001302961.2:c.158G>A	NP_001289890.1:p.Cys53Tyr
NR_126566.2:n.436G>A
NM_004917.5:c.443G>A MANE Select	NP_004908.4:p.Cys148Tyr