Canonical Allele Identifier: CA2586648101

Gene: KLK4

Linked Data

• gnomAD v4: 19-50908204-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908205del , CM000681.2:g.50908205del	GRCh38
NC_000019.9:g.51411461del , CM000681.1:g.51411461del	GRCh37
NC_000019.8:g.56103273del	NCBI36
NG_012154.2:g.7534del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.612+154del MANE Select	ENSP00000326159.1:n.612+154del
ENST00000324041.5:c.612+154del	ENSP00000326159.1:n.612+154del
ENST00000431178.2:c.328+374del	ENSP00000399448.2:n.328+374del
ENST00000593885.1:c.*107+154del	ENSP00000469769.1:n.*107+154del
ENST00000596876.1:n.768del
ENST00000598305.5:c.*107+154del	ENSP00000469963.1:n.*107+154del
ENST00000599865.5:n.548+154del
ENST00000602148.1:c.624+154del	ENSP00000472091.1:n.624+154del
NM_001302961.1:c.327+154del	NP_001289890.1:n.327+154del
NM_004917.4:c.612+154del	NP_004908.4:n.612+154del
NR_126566.1:n.601+154del
XM_005259441.3:c.327+154del	XP_005259498.2:n.327+154del
XM_011527546.1:c.475+374del	XP_011525848.1:n.475+374del
XM_011527547.1:c.465+154del	XP_011525849.1:n.465+154del
XM_005259441.4:c.327+154del	XP_005259498.2:n.327+154del
XM_011527546.2:c.475+374del	XP_011525848.1:n.475+374del
NM_001302961.2:c.327+154del	NP_001289890.1:n.327+154del
NR_126566.2:n.601+154del
NM_004917.5:c.612+154del MANE Select	NP_004908.4:n.612+154del