Canonical Allele Identifier: CA407041477

Gene: KLK4

Linked Data

• dbSNP Id: rs2090456544
• gnomAD v3: 19-50908644-A-G
• gnomAD v4: 19-50908644-A-G
• MyVariant Identifiers: chr19:g.51411900A>G (hg19) ; chr19:g.50908644A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908644A>G , CM000681.2:g.50908644A>G	GRCh38
NC_000019.9:g.51411900A>G , CM000681.1:g.51411900A>G	GRCh37
NC_000019.8:g.56103712A>G	NCBI36
NG_012154.2:g.7095T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.410T>C MANE Select	ENSP00000326159.1:p.Ile137Thr
ENST00000324041.5:c.410T>C	ENSP00000326159.1:p.Ile137Thr
ENST00000431178.2:c.263T>C	ENSP00000399448.2:p.Ile88Thr
ENST00000593885.1:c.125T>C	ENSP00000469769.1:p.Ile42Thr
ENST00000596876.1:n.329T>C
ENST00000598305.5:c.125T>C	ENSP00000469963.1:p.Ile42Thr
ENST00000599865.5:n.263T>C
ENST00000602148.1:c.422T>C	ENSP00000472091.1:n.422T>C
NM_001302961.1:c.125T>C	NP_001289890.1:p.Ile42Thr
NM_004917.4:c.410T>C	NP_004908.4:p.Ile137Thr
NR_126566.1:n.403T>C
XM_005259441.3:c.125T>C	XP_005259498.2:p.Ile42Thr
XM_011527545.1:c.410T>C	XP_011525847.1:p.Ile137Thr
XM_011527546.1:c.410T>C	XP_011525848.1:p.Ile137Thr
XM_011527547.1:c.263T>C	XP_011525849.1:p.Ile88Thr
XM_005259441.4:c.125T>C	XP_005259498.2:p.Ile42Thr
XM_011527545.3:c.410T>C	XP_011525847.1:p.Ile137Thr
XM_011527546.2:c.410T>C	XP_011525848.1:p.Ile137Thr
NM_001302961.2:c.125T>C	NP_001289890.1:p.Ile42Thr
NR_126566.2:n.403T>C
NM_004917.5:c.410T>C MANE Select	NP_004908.4:p.Ile137Thr