Canonical Allele Identifier: CA407041597

Gene: KLK4

Linked Data

• gnomAD v4: 19-50908696-T-C
• MyVariant Identifiers: chr19:g.51411952T>C (hg19) ; chr19:g.50908696T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908696T>C , CM000681.2:g.50908696T>C	GRCh38
NC_000019.9:g.51411952T>C , CM000681.1:g.51411952T>C	GRCh37
NC_000019.8:g.56103764T>C	NCBI36
NG_012154.2:g.7043A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.358A>G MANE Select	ENSP00000326159.1:p.Ile120Val
ENST00000324041.5:c.358A>G	ENSP00000326159.1:p.Ile120Val
ENST00000431178.2:c.211A>G	ENSP00000399448.2:p.Ile71Val
ENST00000593885.1:c.73A>G	ENSP00000469769.1:p.Ile25Val
ENST00000596876.1:n.277A>G
ENST00000598305.5:c.73A>G	ENSP00000469963.1:p.Ile25Val
ENST00000599865.5:n.211A>G
ENST00000602148.1:c.370A>G	ENSP00000472091.1:n.370A>G
NM_001302961.1:c.73A>G	NP_001289890.1:p.Ile25Val
NM_004917.4:c.358A>G	NP_004908.4:p.Ile120Val
NR_126566.1:n.351A>G
XM_005259441.3:c.73A>G	XP_005259498.2:p.Ile25Val
XM_011527545.1:c.358A>G	XP_011525847.1:p.Ile120Val
XM_011527546.1:c.358A>G	XP_011525848.1:p.Ile120Val
XM_011527547.1:c.211A>G	XP_011525849.1:p.Ile71Val
XM_005259441.4:c.73A>G	XP_005259498.2:p.Ile25Val
XM_011527545.3:c.358A>G	XP_011525847.1:p.Ile120Val
XM_011527546.2:c.358A>G	XP_011525848.1:p.Ile120Val
NM_001302961.2:c.73A>G	NP_001289890.1:p.Ile25Val
NR_126566.2:n.351A>G
NM_004917.5:c.358A>G MANE Select	NP_004908.4:p.Ile120Val