Canonical Allele Identifier: CA9605035

Gene: KLK4

Linked Data

• dbSNP Id: rs780404160
• ExAC: 19:51411710 C / T
• gnomAD v2: 19-51411710-C-T
• gnomAD v4: 19-50908454-C-T
• MyVariant Identifiers: chr19:g.51411710C>T (hg19) ; chr19:g.50908454C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908454C>T , CM000681.2:g.50908454C>T	GRCh38
NC_000019.9:g.51411710C>T , CM000681.1:g.51411710C>T	GRCh37
NC_000019.8:g.56103522C>T	NCBI36
NG_012154.2:g.7285G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.517G>A MANE Select	ENSP00000326159.1:p.Val173Met
ENST00000324041.5:c.517G>A	ENSP00000326159.1:p.Val173Met
ENST00000431178.2:c.328+125G>A	ENSP00000399448.2:n.328+125G>A
ENST00000593885.1:c.*12G>A	ENSP00000469769.1:n.*12G>A
ENST00000596876.1:n.519G>A
ENST00000598305.5:c.*12G>A	ENSP00000469963.1:n.*12G>A
ENST00000599865.5:n.453G>A
ENST00000602148.1:c.529G>A	ENSP00000472091.1:n.529G>A
NM_001302961.1:c.232G>A	NP_001289890.1:p.Val78Met
NM_004917.4:c.517G>A	NP_004908.4:p.Val173Met
NR_126566.1:n.506G>A
XM_005259441.3:c.232G>A	XP_005259498.2:p.Val78Met
XM_011527545.1:c.*12G>A	XP_011525847.1:n.*12G>A
XM_011527546.1:c.475+125G>A	XP_011525848.1:n.475+125G>A
XM_011527547.1:c.370G>A	XP_011525849.1:p.Val124Met
XM_005259441.4:c.232G>A	XP_005259498.2:p.Val78Met
XM_011527545.3:c.*12G>A	XP_011525847.1:n.*12G>A
XM_011527546.2:c.475+125G>A	XP_011525848.1:n.475+125G>A
NM_001302961.2:c.232G>A	NP_001289890.1:p.Val78Met
NR_126566.2:n.506G>A
NM_004917.5:c.517G>A MANE Select	NP_004908.4:p.Val173Met