Canonical Allele Identifier: CA508313918

Gene: KLK4

Linked Data

• gnomAD v4: 19-50908817-G-T
• MyVariant Identifiers: chr19:g.51412073G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908817G>T , CM000681.2:g.50908817G>T	GRCh38
NC_000019.9:g.51412073G>T , CM000681.1:g.51412073G>T	GRCh37
NC_000019.8:g.56103885G>T	NCBI36
NG_012154.2:g.6922C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.237C>A MANE Select	ENSP00000326159.1:p.Ile79=
ENST00000324041.5:c.237C>A	ENSP00000326159.1:p.Ile79=
ENST00000431178.2:c.90C>A	ENSP00000399448.2:p.Ile30=
ENST00000593885.1:c.-49C>A	ENSP00000469769.1:n.-49C>A
ENST00000596876.1:n.156C>A
ENST00000598305.5:c.-49C>A	ENSP00000469963.1:n.-49C>A
ENST00000599865.5:n.90C>A
ENST00000602148.1:c.249C>A	ENSP00000472091.1:n.249C>A
NM_001302961.1:c.-49C>A	NP_001289890.1:n.-49C>A
NM_004917.4:c.237C>A	NP_004908.4:p.Ile79=
NR_126566.1:n.230C>A
XM_005259441.3:c.-49C>A	XP_005259498.2:n.-49C>A
XM_011527545.1:c.237C>A	XP_011525847.1:p.Ile79=
XM_011527546.1:c.237C>A	XP_011525848.1:p.Ile79=
XM_011527547.1:c.90C>A	XP_011525849.1:p.Ile30=
XM_005259441.4:c.-49C>A	XP_005259498.2:n.-49C>A
XM_011527545.3:c.237C>A	XP_011525847.1:p.Ile79=
XM_011527546.2:c.237C>A	XP_011525848.1:p.Ile79=
NM_001302961.2:c.-49C>A	NP_001289890.1:n.-49C>A
NR_126566.2:n.230C>A
NM_004917.5:c.237C>A MANE Select	NP_004908.4:p.Ile79=