Canonical Allele Identifier: CA407041725

Gene: KLK4

Linked Data

• dbSNP Id: rs1600047070
• MyVariant Identifiers: chr19:g.51412012T>G (hg19) ; chr19:g.50908756T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908756T>G , CM000681.2:g.50908756T>G	GRCh38
NC_000019.9:g.51412012T>G , CM000681.1:g.51412012T>G	GRCh37
NC_000019.8:g.56103824T>G	NCBI36
NG_012154.2:g.6983A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.298A>C MANE Select	ENSP00000326159.1:p.Ser100Arg
ENST00000324041.5:c.298A>C	ENSP00000326159.1:p.Ser100Arg
ENST00000431178.2:c.151A>C	ENSP00000399448.2:p.Ser51Arg
ENST00000593885.1:c.13A>C	ENSP00000469769.1:p.Ser5Arg
ENST00000596876.1:n.217A>C
ENST00000598305.5:c.13A>C	ENSP00000469963.1:p.Ser5Arg
ENST00000599865.5:n.151A>C
ENST00000602148.1:c.310A>C	ENSP00000472091.1:n.310A>C
NM_001302961.1:c.13A>C	NP_001289890.1:p.Ser5Arg
NM_004917.4:c.298A>C	NP_004908.4:p.Ser100Arg
NR_126566.1:n.291A>C
XM_005259441.3:c.13A>C	XP_005259498.2:p.Ser5Arg
XM_011527545.1:c.298A>C	XP_011525847.1:p.Ser100Arg
XM_011527546.1:c.298A>C	XP_011525848.1:p.Ser100Arg
XM_011527547.1:c.151A>C	XP_011525849.1:p.Ser51Arg
XM_005259441.4:c.13A>C	XP_005259498.2:p.Ser5Arg
XM_011527545.3:c.298A>C	XP_011525847.1:p.Ser100Arg
XM_011527546.2:c.298A>C	XP_011525848.1:p.Ser100Arg
NM_001302961.2:c.13A>C	NP_001289890.1:p.Ser5Arg
NR_126566.2:n.291A>C
NM_004917.5:c.298A>C MANE Select	NP_004908.4:p.Ser100Arg