Canonical Allele Identifier: CA407041468

Gene: KLK4

Linked Data

• ClinVar Variation Id: 2552730
• ClinVar RCV Id: RCV003268914
• MyVariant Identifiers: chr19:g.51411898C>A (hg19) ; chr19:g.50908642C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908642C>A , CM000681.2:g.50908642C>A	GRCh38
NC_000019.9:g.51411898C>A , CM000681.1:g.51411898C>A	GRCh37
NC_000019.8:g.56103710C>A	NCBI36
NG_012154.2:g.7097G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.412G>T MANE Select	ENSP00000326159.1:p.Ala138Ser
ENST00000324041.5:c.412G>T	ENSP00000326159.1:p.Ala138Ser
ENST00000431178.2:c.265G>T	ENSP00000399448.2:p.Ala89Ser
ENST00000593885.1:c.127G>T	ENSP00000469769.1:p.Ala43Ser
ENST00000596876.1:n.331G>T
ENST00000598305.5:c.127G>T	ENSP00000469963.1:p.Ala43Ser
ENST00000599865.5:n.265G>T
ENST00000602148.1:c.424G>T	ENSP00000472091.1:n.424G>T
NM_001302961.1:c.127G>T	NP_001289890.1:p.Ala43Ser
NM_004917.4:c.412G>T	NP_004908.4:p.Ala138Ser
NR_126566.1:n.405G>T
XM_005259441.3:c.127G>T	XP_005259498.2:p.Ala43Ser
XM_011527545.1:c.412G>T	XP_011525847.1:p.Ala138Ser
XM_011527546.1:c.412G>T	XP_011525848.1:p.Ala138Ser
XM_011527547.1:c.265G>T	XP_011525849.1:p.Ala89Ser
XM_005259441.4:c.127G>T	XP_005259498.2:p.Ala43Ser
XM_011527545.3:c.412G>T	XP_011525847.1:p.Ala138Ser
XM_011527546.2:c.412G>T	XP_011525848.1:p.Ala138Ser
NM_001302961.2:c.127G>T	NP_001289890.1:p.Ala43Ser
NR_126566.2:n.405G>T
NM_004917.5:c.412G>T MANE Select	NP_004908.4:p.Ala138Ser