Canonical Allele Identifier: CA407040324

Gene: KLK4

Linked Data

• gnomAD v4: 19-50908374-C-G
• MyVariant Identifiers: chr19:g.51411630C>G (hg19) ; chr19:g.50908374C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908374C>G , CM000681.2:g.50908374C>G	GRCh38
NC_000019.9:g.51411630C>G , CM000681.1:g.51411630C>G	GRCh37
NC_000019.8:g.56103442C>G	NCBI36
NG_012154.2:g.7365G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.597G>C MANE Select	ENSP00000326159.1:p.Gln199His
ENST00000324041.5:c.597G>C	ENSP00000326159.1:p.Gln199His
ENST00000431178.2:c.328+205G>C	ENSP00000399448.2:n.328+205G>C
ENST00000593885.1:c.*92G>C	ENSP00000469769.1:n.*92G>C
ENST00000596876.1:n.599G>C
ENST00000598305.5:c.*92G>C	ENSP00000469963.1:n.*92G>C
ENST00000599865.5:n.533G>C
ENST00000602148.1:c.609G>C	ENSP00000472091.1:n.609G>C
NM_001302961.1:c.312G>C	NP_001289890.1:p.Gln104His
NM_004917.4:c.597G>C	NP_004908.4:p.Gln199His
NR_126566.1:n.586G>C
XM_005259441.3:c.312G>C	XP_005259498.2:p.Gln104His
XM_011527546.1:c.475+205G>C	XP_011525848.1:n.475+205G>C
XM_011527547.1:c.450G>C	XP_011525849.1:p.Gln150His
XM_005259441.4:c.312G>C	XP_005259498.2:p.Gln104His
XM_011527545.3:c.*92G>C	XP_011525847.1:n.*92G>C
XM_011527546.2:c.475+205G>C	XP_011525848.1:n.475+205G>C
NM_001302961.2:c.312G>C	NP_001289890.1:p.Gln104His
NR_126566.2:n.586G>C
NM_004917.5:c.597G>C MANE Select	NP_004908.4:p.Gln199His