Canonical Allele Identifier: CA407041512

Gene: KLK4

Linked Data

• dbSNP Id: rs1309463528
• gnomAD v2: 19-51411913-G-A
• gnomAD v4: 19-50908657-G-A
• COSMIC: COSM1712655
• MyVariant Identifiers: chr19:g.51411913G>A (hg19) ; chr19:g.50908657G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908657G>A , CM000681.2:g.50908657G>A	GRCh38
NC_000019.9:g.51411913G>A , CM000681.1:g.51411913G>A	GRCh37
NC_000019.8:g.56103725G>A	NCBI36
NG_012154.2:g.7082C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.397C>T MANE Select	ENSP00000326159.1:p.Arg133Trp
ENST00000324041.5:c.397C>T	ENSP00000326159.1:p.Arg133Trp
ENST00000431178.2:c.250C>T	ENSP00000399448.2:p.Arg84Trp
ENST00000593885.1:c.112C>T	ENSP00000469769.1:p.Arg38Trp
ENST00000596876.1:n.316C>T
ENST00000598305.5:c.112C>T	ENSP00000469963.1:p.Arg38Trp
ENST00000599865.5:n.250C>T
ENST00000602148.1:c.409C>T	ENSP00000472091.1:n.409C>T
NM_001302961.1:c.112C>T	NP_001289890.1:p.Arg38Trp
NM_004917.4:c.397C>T	NP_004908.4:p.Arg133Trp
NR_126566.1:n.390C>T
XM_005259441.3:c.112C>T	XP_005259498.2:p.Arg38Trp
XM_011527545.1:c.397C>T	XP_011525847.1:p.Arg133Trp
XM_011527546.1:c.397C>T	XP_011525848.1:p.Arg133Trp
XM_011527547.1:c.250C>T	XP_011525849.1:p.Arg84Trp
XM_005259441.4:c.112C>T	XP_005259498.2:p.Arg38Trp
XM_011527545.3:c.397C>T	XP_011525847.1:p.Arg133Trp
XM_011527546.2:c.397C>T	XP_011525848.1:p.Arg133Trp
NM_001302961.2:c.112C>T	NP_001289890.1:p.Arg38Trp
NR_126566.2:n.390C>T
NM_004917.5:c.397C>T MANE Select	NP_004908.4:p.Arg133Trp