Canonical Allele Identifier: CA9605116

Gene: KLK4

Linked Data

• dbSNP Id: rs369572168
• ExAC: 19:51412071 C / T
• gnomAD v2: 19-51412071-C-T
• gnomAD v3: 19-50908815-C-T
• gnomAD v4: 19-50908815-C-T
• MyVariant Identifiers: chr19:g.51412071C>T (hg19) ; chr19:g.50908815C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908815C>T , CM000681.2:g.50908815C>T	GRCh38
NC_000019.9:g.51412071C>T , CM000681.1:g.51412071C>T	GRCh37
NC_000019.8:g.56103883C>T	NCBI36
NG_012154.2:g.6924G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.239G>A MANE Select	ENSP00000326159.1:p.Gly80Glu
ENST00000324041.5:c.239G>A	ENSP00000326159.1:p.Gly80Glu
ENST00000431178.2:c.92G>A	ENSP00000399448.2:p.Gly31Glu
ENST00000593885.1:c.-47G>A	ENSP00000469769.1:n.-47G>A
ENST00000596876.1:n.158G>A
ENST00000598305.5:c.-47G>A	ENSP00000469963.1:n.-47G>A
ENST00000599865.5:n.92G>A
ENST00000602148.1:c.251G>A	ENSP00000472091.1:n.251G>A
NM_001302961.1:c.-47G>A	NP_001289890.1:n.-47G>A
NM_004917.4:c.239G>A	NP_004908.4:p.Gly80Glu
NR_126566.1:n.232G>A
XM_005259441.3:c.-47G>A	XP_005259498.2:n.-47G>A
XM_011527545.1:c.239G>A	XP_011525847.1:p.Gly80Glu
XM_011527546.1:c.239G>A	XP_011525848.1:p.Gly80Glu
XM_011527547.1:c.92G>A	XP_011525849.1:p.Gly31Glu
XM_005259441.4:c.-47G>A	XP_005259498.2:n.-47G>A
XM_011527545.3:c.239G>A	XP_011525847.1:p.Gly80Glu
XM_011527546.2:c.239G>A	XP_011525848.1:p.Gly80Glu
NM_001302961.2:c.-47G>A	NP_001289890.1:n.-47G>A
NR_126566.2:n.232G>A
NM_004917.5:c.239G>A MANE Select	NP_004908.4:p.Gly80Glu