Canonical Allele Identifier: CA9605174

Gene: KLK4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50909410C>A , CM000681.2:g.50909410C>A	GRCh38
NC_000019.9:g.51412666C>A , CM000681.1:g.51412666C>A	GRCh37
NC_000019.8:g.56104478C>A	NCBI36
NG_012154.2:g.6329G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.66G>T MANE Select	ENSP00000326159.1:p.Ser22=
ENST00000324041.5:c.66G>T	ENSP00000326159.1:p.Ser22=
ENST00000598305.5:c.-217-15G>T	ENSP00000469963.1:n.-217-15G>T
ENST00000602148.1:c.66G>T	ENSP00000472091.1:p.Ser22=
NM_001302961.1:c.-232G>T	NP_001289890.1:n.-232G>T
NM_004917.4:c.66G>T	NP_004908.4:p.Ser22=
NR_126566.1:n.62-15G>T
XM_011527545.1:c.66G>T	XP_011525847.1:p.Ser22=
XM_011527546.1:c.66G>T	XP_011525848.1:p.Ser22=
XM_011527547.1:c.-67-15G>T	XP_011525849.1:n.-67-15G>T
XM_011527545.3:c.66G>T	XP_011525847.1:p.Ser22=
XM_011527546.2:c.66G>T	XP_011525848.1:p.Ser22=
NM_001302961.2:c.-232G>T	NP_001289890.1:n.-232G>T
NR_126566.2:n.62-15G>T
NM_004917.5:c.66G>T MANE Select	NP_004908.4:p.Ser22=