Canonical Allele Identifier: CA2341138419

Gene: KLK4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908716_50908722delinsAGCAAGG , CM000681.2:g.50908716_50908722delinsAGCAAGG	GRCh38
NC_000019.9:g.51411972_51411978delinsAGCAAGG , CM000681.1:g.51411972_51411978delinsAGCAAGG	GRCh37
NC_000019.8:g.56103784_56103790delinsAGCAAGG	NCBI36
NG_012154.2:g.7017_7023delinsCCTTGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.332_338delinsCCTTGCT MANE Select	ENSP00000326159.1:p.Pro111=
ENST00000324041.5:c.332_338delinsCCTTGCT	ENSP00000326159.1:p.Pro111=
ENST00000431178.2:c.185_191delinsCCTTGCT	ENSP00000399448.2:p.Pro62=
ENST00000593885.1:c.47_53delinsCCTTGCT	ENSP00000469769.1:p.Pro16=
ENST00000596876.1:n.251_257delinsCCTTGCT
ENST00000598305.5:c.47_53delinsCCTTGCT	ENSP00000469963.1:p.Pro16=
ENST00000599865.5:n.185_191delinsCCTTGCT
ENST00000602148.1:c.344_350delinsCCTTGCT	ENSP00000472091.1:n.344_350delinsCCTTGCT
NM_001302961.1:c.47_53delinsCCTTGCT	NP_001289890.1:p.Pro16=
NM_004917.4:c.332_338delinsCCTTGCT	NP_004908.4:p.Pro111=
NR_126566.1:n.325_331delinsCCTTGCT
XM_005259441.3:c.47_53delinsCCTTGCT	XP_005259498.2:p.Pro16=
XM_011527545.1:c.332_338delinsCCTTGCT	XP_011525847.1:p.Pro111=
XM_011527546.1:c.332_338delinsCCTTGCT	XP_011525848.1:p.Pro111=
XM_011527547.1:c.185_191delinsCCTTGCT	XP_011525849.1:p.Pro62=
XM_005259441.4:c.47_53delinsCCTTGCT	XP_005259498.2:p.Pro16=
XM_011527545.3:c.332_338delinsCCTTGCT	XP_011525847.1:p.Pro111=
XM_011527546.2:c.332_338delinsCCTTGCT	XP_011525848.1:p.Pro111=
NM_001302961.2:c.47_53delinsCCTTGCT	NP_001289890.1:p.Pro16=
NR_126566.2:n.325_331delinsCCTTGCT
NM_004917.5:c.332_338delinsCCTTGCT MANE Select	NP_004908.4:p.Pro111=