Canonical Allele Identifier: CA633899585

Gene: KLK4

Linked Data

• dbSNP Id: rs117475014
• gnomAD v2: 19-51412122-C-A
• gnomAD v4: 19-50908866-C-A
• MyVariant Identifiers: chr19:g.51412122C>A (hg19) ; chr19:g.50908866C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908866C>A , CM000681.2:g.50908866C>A	GRCh38
NC_000019.9:g.51412122C>A , CM000681.1:g.51412122C>A	GRCh37
NC_000019.8:g.56103934C>A	NCBI36
NG_012154.2:g.6873G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.225-37G>T MANE Select	ENSP00000326159.1:n.225-37G>T
ENST00000324041.5:c.225-37G>T	ENSP00000326159.1:n.225-37G>T
ENST00000431178.2:c.78-37G>T	ENSP00000399448.2:n.78-37G>T
ENST00000593885.1:c.-61-37G>T	ENSP00000469769.1:n.-61-37G>T
ENST00000596876.1:n.144-37G>T
ENST00000598305.5:c.-61-37G>T	ENSP00000469963.1:n.-61-37G>T
ENST00000599865.5:n.78-37G>T
ENST00000602148.1:c.237-37G>T	ENSP00000472091.1:n.237-37G>T
NM_001302961.1:c.-61-37G>T	NP_001289890.1:n.-61-37G>T
NM_004917.4:c.225-37G>T	NP_004908.4:n.225-37G>T
NR_126566.1:n.218-37G>T
XM_005259441.3:c.-61-37G>T	XP_005259498.2:n.-61-37G>T
XM_011527545.1:c.225-37G>T	XP_011525847.1:n.225-37G>T
XM_011527546.1:c.225-37G>T	XP_011525848.1:n.225-37G>T
XM_011527547.1:c.78-37G>T	XP_011525849.1:n.78-37G>T
XM_005259441.4:c.-61-37G>T	XP_005259498.2:n.-61-37G>T
XM_011527545.3:c.225-37G>T	XP_011525847.1:n.225-37G>T
XM_011527546.2:c.225-37G>T	XP_011525848.1:n.225-37G>T
NM_001302961.2:c.-61-37G>T	NP_001289890.1:n.-61-37G>T
NR_126566.2:n.218-37G>T
NM_004917.5:c.225-37G>T MANE Select	NP_004908.4:n.225-37G>T