Canonical Allele Identifier: CA996838579

Gene: KLK4

Linked Data

• gnomAD v3: 19-50908132-T-TGTGTGAAAATGCTGTTGGAAGGTCAACTGCATTTCTAC
• gnomAD v4: 19-50908132-T-TGTGTGAAAATGCTGTTGGAAGGTCAACTGCATTTCTAC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908137_50908138insAAAATGCTGTTGGAAGGTCAACTGCATTTCTACGTGTG , CM000681.2:g.50908137_50908138insAAAATGCTGTTGGAAGGTCAACTGCATTTCTACGTGTG	GRCh38
NC_000019.9:g.51411393_51411394insAAAATGCTGTTGGAAGGTCAACTGCATTTCTACGTGTG , CM000681.1:g.51411393_51411394insAAAATGCTGTTGGAAGGTCAACTGCATTTCTACGTGTG	GRCh37
NC_000019.8:g.56103205_56103206insAAAATGCTGTTGGAAGGTCAACTGCATTTCTACGTGTG	NCBI36
NG_012154.2:g.7606_7607insGTAGAAATGCAGTTGACCTTCCAACAGCATTTTCACAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.612+226_612+227insGTAGAAATGCAGTTGACCTTCCAACAGCATTTTCACAC MANE Select	ENSP00000326159.1:n.612+226_612+227insGTAGAAATGCAGTTGACCTTCCA...
ENST00000324041.5:c.612+226_612+227insGTAGAAATGCAGTTGACCTTCCAACAGCATTTTCACAC	ENSP00000326159.1:n.612+226_612+227insGTAGAAATGCAGTTGACCTTCCA...
ENST00000431178.2:c.328+446_328+447insGTAGAAATGCAGTTGACCTTCCAACAGCATTTTCACAC	ENSP00000399448.2:n.328+446_328+447insGTAGAAATGCAGTTGACCTTCCA...
ENST00000593885.1:c.*107+226_*107+227insGTAGAAATGCAGTTGACCTTCCAACAGCATTTTCACAC	ENSP00000469769.1:n.*107+226_*107+227insGTAGAAATGCAGTTGACCTTC...
ENST00000596876.1:n.840_841insGTAGAAATGCAGTTGACCTTCCAACAGCATTTTCACAC
ENST00000598305.5:c.*107+226_*107+227insGTAGAAATGCAGTTGACCTTCCAACAGCATTTTCACAC	ENSP00000469963.1:n.*107+226_*107+227insGTAGAAATGCAGTTGACCTTC...
ENST00000599865.5:n.548+226_548+227insGTAGAAATGCAGTTGACCTTCCAACAGCATTTTCACAC
ENST00000602148.1:c.624+226_624+227insGTAGAAATGCAGTTGACCTTCCAACAGCATTTTCACAC	ENSP00000472091.1:n.624+226_624+227insGTAGAAATGCAGTTGACCTTCCA...
NM_001302961.1:c.327+226_327+227insGTAGAAATGCAGTTGACCTTCCAACAGCATTTTCACAC	NP_001289890.1:n.327+226_327+227insGTAGAAATGCAGTTGACCTTCCAACA...
NM_004917.4:c.612+226_612+227insGTAGAAATGCAGTTGACCTTCCAACAGCATTTTCACAC	NP_004908.4:n.612+226_612+227insGTAGAAATGCAGTTGACCTTCCAACAGCA...
NR_126566.1:n.601+226_601+227insGTAGAAATGCAGTTGACCTTCCAACAGCATTTTCACAC
XM_005259441.3:c.327+226_327+227insGTAGAAATGCAGTTGACCTTCCAACAGCATTTTCACAC	XP_005259498.2:n.327+226_327+227insGTAGAAATGCAGTTGACCTTCCAACA...
XM_011527546.1:c.475+446_475+447insGTAGAAATGCAGTTGACCTTCCAACAGCATTTTCACAC	XP_011525848.1:n.475+446_475+447insGTAGAAATGCAGTTGACCTTCCAACA...
XM_011527547.1:c.465+226_465+227insGTAGAAATGCAGTTGACCTTCCAACAGCATTTTCACAC	XP_011525849.1:n.465+226_465+227insGTAGAAATGCAGTTGACCTTCCAACA...
XM_005259441.4:c.327+226_327+227insGTAGAAATGCAGTTGACCTTCCAACAGCATTTTCACAC	XP_005259498.2:n.327+226_327+227insGTAGAAATGCAGTTGACCTTCCAACA...
XM_011527546.2:c.475+446_475+447insGTAGAAATGCAGTTGACCTTCCAACAGCATTTTCACAC	XP_011525848.1:n.475+446_475+447insGTAGAAATGCAGTTGACCTTCCAACA...
NM_001302961.2:c.327+226_327+227insGTAGAAATGCAGTTGACCTTCCAACAGCATTTTCACAC	NP_001289890.1:n.327+226_327+227insGTAGAAATGCAGTTGACCTTCCAACA...
NR_126566.2:n.601+226_601+227insGTAGAAATGCAGTTGACCTTCCAACAGCATTTTCACAC
NM_004917.5:c.612+226_612+227insGTAGAAATGCAGTTGACCTTCCAACAGCATTTTCACAC MANE Select	NP_004908.4:n.612+226_612+227insGTAGAAATGCAGTTGACCTTCCAACAGCA...