Canonical Allele Identifier: CA407041178

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411743G>T (hg19) ; chr19:g.50908487G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908487G>T , CM000681.2:g.50908487G>T	GRCh38
NC_000019.9:g.51411743G>T , CM000681.1:g.51411743G>T	GRCh37
NC_000019.8:g.56103555G>T	NCBI36
NG_012154.2:g.7252C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.484C>A MANE Select	ENSP00000326159.1:p.Pro162Thr
ENST00000324041.5:c.484C>A	ENSP00000326159.1:p.Pro162Thr
ENST00000431178.2:c.328+92C>A	ENSP00000399448.2:n.328+92C>A
ENST00000593885.1:c.195C>A	ENSP00000469769.1:p.Cys65Ter
ENST00000596876.1:n.486C>A
ENST00000598305.5:c.195C>A	ENSP00000469963.1:p.Cys65Ter
ENST00000599865.5:n.420C>A
ENST00000602148.1:c.496C>A	ENSP00000472091.1:n.496C>A
NM_001302961.1:c.199C>A	NP_001289890.1:p.Pro67Thr
NM_004917.4:c.484C>A	NP_004908.4:p.Pro162Thr
NR_126566.1:n.473C>A
XM_005259441.3:c.199C>A	XP_005259498.2:p.Pro67Thr
XM_011527545.1:c.480C>A	XP_011525847.1:p.Cys160Ter
XM_011527546.1:c.475+92C>A	XP_011525848.1:n.475+92C>A
XM_011527547.1:c.337C>A	XP_011525849.1:p.Pro113Thr
XM_005259441.4:c.199C>A	XP_005259498.2:p.Pro67Thr
XM_011527545.3:c.480C>A	XP_011525847.1:p.Cys160Ter
XM_011527546.2:c.475+92C>A	XP_011525848.1:n.475+92C>A
NM_001302961.2:c.199C>A	NP_001289890.1:p.Pro67Thr
NR_126566.2:n.473C>A
NM_004917.5:c.484C>A MANE Select	NP_004908.4:p.Pro162Thr